Canonical Allele Identifier: CA2581416616

Gene: LIMCH1

Linked Data

• dbSNP Id: rs4345220

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.41637499A>T , CM000666.2:g.41637499A>T	GRCh38
NC_000004.11:g.41639516A>T , CM000666.1:g.41639516A>T	GRCh37
NC_000004.10:g.41334273A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000313860.12:c.936-1433A>T	ENSP00000316891.7:n.936-1433A>T
ENST00000503057.6:c.2091-1433A>T MANE Select	ENSP00000425631.1:n.2091-1433A>T
ENST00000313860.11:c.936-1433A>T	ENSP00000316891.7:n.936-1433A>T
ENST00000381753.8:c.474-7001A>T	ENSP00000371172.4:n.474-7001A>T
ENST00000396595.7:c.474-1433A>T	ENSP00000379840.3:n.474-1433A>T
ENST00000503057.5:c.2091-1433A>T	ENSP00000425631.1:n.2091-1433A>T
ENST00000508466.1:c.440-1433A>T
ENST00000508501.5:c.936-1433A>T	ENSP00000424825.1:n.936-1433A>T
ENST00000509277.5:c.474-7001A>T	ENSP00000422864.1:n.474-7001A>T
ENST00000511496.5:c.459-1433A>T	ENSP00000421242.1:n.459-1433A>T
ENST00000512632.5:c.936-1433A>T	ENSP00000427045.1:n.936-1433A>T
ENST00000512820.5:c.936-7001A>T	ENSP00000424437.1:n.936-7001A>T
ENST00000512946.5:c.936-1433A>T	ENSP00000424645.1:n.936-1433A>T
ENST00000513024.5:c.459-7001A>T	ENSP00000425222.1:n.459-7001A>T
ENST00000514096.5:c.495-7001A>T	ENSP00000426334.1:n.495-7001A>T
NM_001112717.2:c.936-1433A>T	NP_001106188.1:n.936-1433A>T
NM_001112718.2:c.936-1433A>T	NP_001106189.1:n.936-1433A>T
NM_001112719.2:c.474-1433A>T	NP_001106190.1:n.474-1433A>T
NM_001112720.2:c.474-7001A>T	NP_001106191.1:n.474-7001A>T
NM_001289122.1:c.936-7001A>T	NP_001276051.1:n.936-7001A>T
NM_001289124.1:c.459-7001A>T	NP_001276053.1:n.459-7001A>T
NM_014988.3:c.936-1433A>T	NP_055803.2:n.936-1433A>T
XM_005248057.1:c.2568-1433A>T	XP_005248114.1:n.2568-1433A>T
XM_005248058.1:c.2568-1433A>T	XP_005248115.1:n.2568-1433A>T
XM_005248060.1:c.2568-1433A>T	XP_005248117.1:n.2568-1433A>T
XM_005248061.1:c.2568-1433A>T	XP_005248118.1:n.2568-1433A>T
XM_005248067.1:c.2091-1433A>T	XP_005248124.1:n.2091-1433A>T
XM_005248072.1:c.936-1433A>T	XP_005248129.1:n.936-1433A>T
XM_005248074.1:c.936-7001A>T	XP_005248131.1:n.936-7001A>T
XM_005248075.1:c.936-7001A>T	XP_005248132.1:n.936-7001A>T
XM_006713996.1:c.2568-1433A>T	XP_006714059.1:n.2568-1433A>T
XM_011513642.1:c.2568-1433A>T	XP_011511944.1:n.2568-1433A>T
XM_011513643.1:c.2568-1433A>T	XP_011511945.1:n.2568-1433A>T
XM_011513644.1:c.2568-1433A>T	XP_011511946.1:n.2568-1433A>T
XM_011513645.1:c.2568-1433A>T	XP_011511947.1:n.2568-1433A>T
XM_011513646.1:c.2568-1433A>T	XP_011511948.1:n.2568-1433A>T
XM_011513648.1:c.2325-1433A>T	XP_011511950.1:n.2325-1433A>T
XM_011513649.1:c.2106-1433A>T	XP_011511951.1:n.2106-1433A>T
XM_011513650.1:c.2091-1433A>T	XP_011511952.1:n.2091-1433A>T
XM_011513651.1:c.2091-1433A>T	XP_011511953.1:n.2091-1433A>T
XM_011513652.1:c.1995-1433A>T	XP_011511954.1:n.1995-1433A>T
XM_011513653.1:c.936-1433A>T	XP_011511955.1:n.936-1433A>T
XM_011513654.1:c.936-7001A>T	XP_011511956.1:n.936-7001A>T
XM_011513655.1:c.474-7001A>T	XP_011511957.1:n.474-7001A>T
XM_011513656.1:c.474-1433A>T	XP_011511958.1:n.474-1433A>T
XM_011513657.1:c.474-7001A>T	XP_011511959.1:n.474-7001A>T
XM_011513658.1:c.459-7001A>T	XP_011511960.1:n.459-7001A>T
NM_001112717.3:c.936-1433A>T	NP_001106188.1:n.936-1433A>T
NM_001112718.3:c.936-1433A>T	NP_001106189.1:n.936-1433A>T
NM_001112719.3:c.474-1433A>T	NP_001106190.1:n.474-1433A>T
NM_001112720.3:c.474-7001A>T	NP_001106191.1:n.474-7001A>T
NM_001289122.2:c.936-7001A>T	NP_001276051.1:n.936-7001A>T
NM_001330672.1:c.2091-1433A>T	NP_001317601.1:n.2091-1433A>T
NM_001330674.1:c.474-7001A>T	NP_001317603.1:n.474-7001A>T
NM_001330784.1:c.936-1433A>T	NP_001317713.1:n.936-1433A>T
NM_001330786.1:c.459-1433A>T	NP_001317715.1:n.459-1433A>T
NM_001330787.1:c.936-1433A>T	NP_001317716.1:n.936-1433A>T
NM_001330788.1:c.936-1433A>T	NP_001317717.1:n.936-1433A>T
NM_001330789.1:c.936-1433A>T	NP_001317718.1:n.936-1433A>T
NM_001330790.1:c.936-1433A>T	NP_001317719.1:n.936-1433A>T
NM_001330791.1:c.936-7001A>T	NP_001317720.1:n.936-7001A>T
NM_001330792.1:c.936-7001A>T	NP_001317721.1:n.936-7001A>T
NM_001330793.1:c.474-1433A>T	NP_001317722.1:n.474-1433A>T
NM_001330982.1:c.474-1433A>T	NP_001317911.1:n.474-1433A>T
NM_001330983.1:c.474-1433A>T	NP_001317912.1:n.474-1433A>T
NM_014988.4:c.936-1433A>T	NP_055803.2:n.936-1433A>T
XM_011513651.2:c.2091-1433A>T	XP_011511953.1:n.2091-1433A>T
XM_017007894.1:c.2568-1433A>T	XP_016863383.1:n.2568-1433A>T
XM_017007895.1:c.2568-1433A>T	XP_016863384.1:n.2568-1433A>T
XM_017007896.1:c.2568-1433A>T	XP_016863385.1:n.2568-1433A>T
XM_017007897.1:c.2568-1433A>T	XP_016863386.1:n.2568-1433A>T
XM_017007898.1:c.936-1433A>T	XP_016863387.1:n.936-1433A>T
XM_017007900.1:c.936-1433A>T	XP_016863389.1:n.936-1433A>T
XM_017007903.1:c.474-1433A>T	XP_016863392.1:n.474-1433A>T
XM_024453937.1:c.936-7001A>T	XP_024309705.1:n.936-7001A>T
XM_024453938.1:c.474-1433A>T	XP_024309706.1:n.474-1433A>T
NM_001330672.2:c.2091-1433A>T MANE Select	NP_001317601.1:n.2091-1433A>T
NM_001112717.4:c.936-1433A>T	NP_001106188.1:n.936-1433A>T
NM_001112718.4:c.936-1433A>T	NP_001106189.1:n.936-1433A>T
NM_001289122.3:c.936-7001A>T	NP_001276051.1:n.936-7001A>T
NM_001289124.2:c.459-7001A>T	NP_001276053.1:n.459-7001A>T
NM_001330784.2:c.936-1433A>T	NP_001317713.1:n.936-1433A>T
NM_001330786.2:c.459-1433A>T	NP_001317715.1:n.459-1433A>T
NM_001330787.2:c.936-1433A>T	NP_001317716.1:n.936-1433A>T
NM_001330788.2:c.936-1433A>T	NP_001317717.1:n.936-1433A>T
NM_001330789.2:c.936-1433A>T	NP_001317718.1:n.936-1433A>T
NM_001330790.2:c.936-1433A>T	NP_001317719.1:n.936-1433A>T
NM_001330791.2:c.936-7001A>T	NP_001317720.1:n.936-7001A>T
NM_001330792.2:c.936-7001A>T	NP_001317721.1:n.936-7001A>T
NM_014988.5:c.936-1433A>T	NP_055803.2:n.936-1433A>T
NM_001112719.4:c.474-1433A>T	NP_001106190.1:n.474-1433A>T
NM_001112720.4:c.474-7001A>T	NP_001106191.1:n.474-7001A>T
NM_001330674.2:c.474-7001A>T	NP_001317603.1:n.474-7001A>T
NM_001330793.2:c.474-1433A>T	NP_001317722.1:n.474-1433A>T
NM_001330982.2:c.474-1433A>T	NP_001317911.1:n.474-1433A>T