Canonical Allele Identifier: CA345374878

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237015897G>C (hg19) ; chr1:g.236852597G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852597G>C , CM000663.2:g.236852597G>C	GRCh38
NC_000001.10:g.237015897G>C , CM000663.1:g.237015897G>C	GRCh37
NC_000001.9:g.235082520G>C	NCBI36
NG_008959.1:g.62317G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1772G>C MANE Select	ENSP00000355536.5:p.Arg591Pro
ENST00000535889.6:c.1772G>C	ENSP00000441845.1:p.Arg591Pro
ENST00000650888.1:c.*814G>C	ENSP00000498393.1:n.*814G>C
ENST00000651455.1:c.*516G>C	ENSP00000498963.1:n.*516G>C
ENST00000674797.2:c.1424G>C	ENSP00000502299.2:p.Arg475Pro
ENST00000679569.1:n.2086G>C
ENST00000679842.1:c.1772G>C	ENSP00000506109.1:p.Arg591Pro
ENST00000680454.1:n.2216G>C
ENST00000681102.1:c.1592G>C	ENSP00000505600.1:p.Arg531Pro
ENST00000681177.1:c.1516-7236G>C	ENSP00000506327.1:n.1516-7236G>C
ENST00000681937.1:n.2148-7236G>C
ENST00000366576.3:c.434G>C	ENSP00000355535.3:p.Arg145Pro
ENST00000366577.9:c.1772G>C	ENSP00000355536.5:p.Arg591Pro
ENST00000463959.1:n.1791G>C
ENST00000535889.5:c.1772G>C	ENSP00000441845.1:p.Arg591Pro
NM_000254.2:c.1772G>C	NP_000245.2:p.Arg591Pro
NM_001291939.1:c.1772G>C	NP_001278868.1:p.Arg591Pro
NM_001291940.1:c.551G>C	NP_001278869.1:p.Arg184Pro
XM_005273141.3:c.1769G>C	XP_005273198.1:p.Arg590Pro
XM_006711769.2:c.1772G>C	XP_006711832.1:p.Arg591Pro
XM_006711770.1:c.836G>C	XP_006711833.1:p.Arg279Pro
XM_011544193.1:c.1772G>C	XP_011542495.1:p.Arg591Pro
XM_011544194.1:c.1940G>C	XP_011542496.1:p.Arg647Pro
XM_005273141.5:c.1769G>C	XP_005273198.1:p.Arg590Pro
XM_006711770.3:c.836G>C	XP_006711833.1:p.Arg279Pro
XM_011544194.3:c.1940G>C	XP_011542496.1:p.Arg647Pro
XM_017001329.2:c.1940G>C	XP_016856818.1:p.Arg647Pro
XM_017001330.2:c.1940G>C	XP_016856819.1:p.Arg647Pro
NM_001291940.2:c.551G>C	NP_001278869.1:p.Arg184Pro
NM_000254.3:c.1772G>C MANE Select	NP_000245.2:p.Arg591Pro