Canonical Allele Identifier: CA345375016

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237016258A>C (hg19) ; chr1:g.236852958A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852958A>C , CM000663.2:g.236852958A>C	GRCh38
NC_000001.10:g.237016258A>C , CM000663.1:g.237016258A>C	GRCh37
NC_000001.9:g.235082881A>C	NCBI36
NG_008959.1:g.62678A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1823A>C MANE Select	ENSP00000355536.5:p.Asp608Ala
ENST00000535889.6:c.1823A>C	ENSP00000441845.1:p.Asp608Ala
ENST00000650888.1:c.*865A>C	ENSP00000498393.1:n.*865A>C
ENST00000651455.1:c.*567A>C	ENSP00000498963.1:n.*567A>C
ENST00000674797.2:c.1475A>C	ENSP00000502299.2:p.Asp492Ala
ENST00000679569.1:n.2137A>C
ENST00000679842.1:c.1823A>C	ENSP00000506109.1:p.Asp608Ala
ENST00000680454.1:n.2267A>C
ENST00000681102.1:c.1643A>C	ENSP00000505600.1:p.Asp548Ala
ENST00000681177.1:c.1516-6875A>C	ENSP00000506327.1:n.1516-6875A>C
ENST00000681937.1:n.2148-6875A>C
ENST00000366576.3:c.485A>C	ENSP00000355535.3:p.Asp162Ala
ENST00000366577.9:c.1823A>C	ENSP00000355536.5:p.Asp608Ala
ENST00000463959.1:n.1842A>C
ENST00000535889.5:c.1823A>C	ENSP00000441845.1:p.Asp608Ala
NM_000254.2:c.1823A>C	NP_000245.2:p.Asp608Ala
NM_001291939.1:c.1823A>C	NP_001278868.1:p.Asp608Ala
NM_001291940.1:c.602A>C	NP_001278869.1:p.Asp201Ala
XM_005273141.3:c.1820A>C	XP_005273198.1:p.Asp607Ala
XM_006711769.2:c.1823A>C	XP_006711832.1:p.Asp608Ala
XM_006711770.1:c.887A>C	XP_006711833.1:p.Asp296Ala
XM_011544193.1:c.1823A>C	XP_011542495.1:p.Asp608Ala
XM_011544194.1:c.1991A>C	XP_011542496.1:p.Asp664Ala
XM_005273141.5:c.1820A>C	XP_005273198.1:p.Asp607Ala
XM_006711770.3:c.887A>C	XP_006711833.1:p.Asp296Ala
XM_011544194.3:c.1991A>C	XP_011542496.1:p.Asp664Ala
XM_017001329.2:c.1991A>C	XP_016856818.1:p.Asp664Ala
XM_017001330.2:c.1991A>C	XP_016856819.1:p.Asp664Ala
NM_001291940.2:c.602A>C	NP_001278869.1:p.Asp201Ala
NM_000254.3:c.1823A>C MANE Select	NP_000245.2:p.Asp608Ala