Canonical Allele Identifier: CA345384683

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237048510G>C (hg19) ; chr1:g.236885210G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885210G>C , CM000663.2:g.236885210G>C	GRCh38
NC_000001.10:g.237048510G>C , CM000663.1:g.237048510G>C	GRCh37
NC_000001.9:g.235115133G>C	NCBI36
NG_008959.1:g.94930G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.2766G>C MANE Select	ENSP00000355536.5:p.Glu922Asp
ENST00000535889.6:c.2613G>C	ENSP00000441845.1:p.Glu871Asp
ENST00000650888.1:c.*1808G>C	ENSP00000498393.1:n.*1808G>C
ENST00000651455.1:c.*1510G>C	ENSP00000498963.1:n.*1510G>C
ENST00000674797.2:c.2418G>C	ENSP00000502299.2:p.Glu806Asp
ENST00000679569.1:n.3080G>C
ENST00000679842.1:c.2577G>C	ENSP00000506109.1:p.Glu859Asp
ENST00000680454.1:n.3210G>C
ENST00000681102.1:c.2586G>C	ENSP00000505600.1:p.Glu862Asp
ENST00000681177.1:c.2328G>C	ENSP00000506327.1:p.Glu776Asp
ENST00000681937.1:n.2960G>C
ENST00000366576.3:c.1428G>C	ENSP00000355535.3:p.Glu476Asp
ENST00000366577.9:c.2766G>C	ENSP00000355536.5:p.Glu922Asp
ENST00000535889.5:c.2613G>C	ENSP00000441845.1:p.Glu871Asp
NM_000254.2:c.2766G>C	NP_000245.2:p.Glu922Asp
NM_001291939.1:c.2613G>C	NP_001278868.1:p.Glu871Asp
NM_001291940.1:c.1545G>C	NP_001278869.1:p.Glu515Asp
XM_005273141.3:c.2763G>C	XP_005273198.1:p.Glu921Asp
XM_006711769.2:c.2766G>C	XP_006711832.1:p.Glu922Asp
XM_006711770.1:c.1830G>C	XP_006711833.1:p.Glu610Asp
XM_011544193.1:c.2577G>C	XP_011542495.1:p.Glu859Asp
XM_011544194.1:c.2934G>C	XP_011542496.1:p.Glu978Asp
XM_005273141.5:c.2763G>C	XP_005273198.1:p.Glu921Asp
XM_006711770.3:c.1830G>C	XP_006711833.1:p.Glu610Asp
XM_011544194.3:c.2934G>C	XP_011542496.1:p.Glu978Asp
XM_017001329.2:c.2781G>C	XP_016856818.1:p.Glu927Asp
XM_017001330.2:c.2745G>C	XP_016856819.1:p.Glu915Asp
NM_001291940.2:c.1545G>C	NP_001278869.1:p.Glu515Asp
NM_000254.3:c.2766G>C MANE Select	NP_000245.2:p.Glu922Asp