Canonical Allele Identifier: CA2487101857

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236880840A= , CM000663.2:g.236880840A=	GRCh38
NC_000001.10:g.237044140A= , CM000663.1:g.237044140A=	GRCh37
NC_000001.9:g.235110763A=	NCBI36
NG_008959.1:g.90560A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.2676+4A= MANE Select	ENSP00000355536.5:n.2676+4A=
ENST00000535889.6:c.2523+4A=	ENSP00000441845.1:n.2523+4A=
ENST00000650888.1:c.*1718+4A=	ENSP00000498393.1:n.*1718+4A=
ENST00000651455.1:c.*1420+4A=	ENSP00000498963.1:n.*1420+4A=
ENST00000674797.2:c.2328+4A=	ENSP00000502299.2:n.2328+4A=
ENST00000679569.1:n.2990+4A=
ENST00000679842.1:c.2487+4A=	ENSP00000506109.1:n.2487+4A=
ENST00000680454.1:n.3120+4A=
ENST00000681102.1:c.2496+4A=	ENSP00000505600.1:n.2496+4A=
ENST00000681177.1:c.2238+4A=	ENSP00000506327.1:n.2238+4A=
ENST00000681937.1:n.2870+4A=
ENST00000366576.3:c.1338+4A=	ENSP00000355535.3:n.1338+4A=
ENST00000366577.9:c.2676+4A=	ENSP00000355536.5:n.2676+4A=
ENST00000535889.5:c.2523+4A=	ENSP00000441845.1:n.2523+4A=
NM_000254.2:c.2676+4A=	NP_000245.2:n.2676+4A=
NM_001291939.1:c.2523+4A=	NP_001278868.1:n.2523+4A=
NM_001291940.1:c.1455+4A=	NP_001278869.1:n.1455+4A=
XM_005273141.3:c.2673+4A=	XP_005273198.1:n.2673+4A=
XM_006711769.2:c.2676+4A=	XP_006711832.1:n.2676+4A=
XM_006711770.1:c.1740+4A=	XP_006711833.1:n.1740+4A=
XM_011544193.1:c.2487+4A=	XP_011542495.1:n.2487+4A=
XM_011544194.1:c.2844+4A=	XP_011542496.1:n.2844+4A=
XM_005273141.5:c.2673+4A=	XP_005273198.1:n.2673+4A=
XM_006711770.3:c.1740+4A=	XP_006711833.1:n.1740+4A=
XM_011544194.3:c.2844+4A=	XP_011542496.1:n.2844+4A=
XM_017001329.2:c.2691+4A=	XP_016856818.1:n.2691+4A=
XM_017001330.2:c.2655+4A=	XP_016856819.1:n.2655+4A=
NM_001291940.2:c.1455+4A=	NP_001278869.1:n.1455+4A=
NM_000254.3:c.2676+4A= MANE Select	NP_000245.2:n.2676+4A=