Canonical Allele Identifier: CA345384396

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237048437A>T (hg19) ; chr1:g.236885137A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885137A>T , CM000663.2:g.236885137A>T	GRCh38
NC_000001.10:g.237048437A>T , CM000663.1:g.237048437A>T	GRCh37
NC_000001.9:g.235115060A>T	NCBI36
NG_008959.1:g.94857A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.2693A>T MANE Select	ENSP00000355536.5:p.Asp898Val
ENST00000535889.6:c.2540A>T	ENSP00000441845.1:p.Asp847Val
ENST00000650888.1:c.*1735A>T	ENSP00000498393.1:n.*1735A>T
ENST00000651455.1:c.*1437A>T	ENSP00000498963.1:n.*1437A>T
ENST00000674797.2:c.2345A>T	ENSP00000502299.2:p.Asp782Val
ENST00000679569.1:n.3007A>T
ENST00000679842.1:c.2504A>T	ENSP00000506109.1:p.Asp835Val
ENST00000680454.1:n.3137A>T
ENST00000681102.1:c.2513A>T	ENSP00000505600.1:p.Asp838Val
ENST00000681177.1:c.2255A>T	ENSP00000506327.1:p.Asp752Val
ENST00000681937.1:n.2887A>T
ENST00000366576.3:c.1355A>T	ENSP00000355535.3:p.Asp452Val
ENST00000366577.9:c.2693A>T	ENSP00000355536.5:p.Asp898Val
ENST00000535889.5:c.2540A>T	ENSP00000441845.1:p.Asp847Val
NM_000254.2:c.2693A>T	NP_000245.2:p.Asp898Val
NM_001291939.1:c.2540A>T	NP_001278868.1:p.Asp847Val
NM_001291940.1:c.1472A>T	NP_001278869.1:p.Asp491Val
XM_005273141.3:c.2690A>T	XP_005273198.1:p.Asp897Val
XM_006711769.2:c.2693A>T	XP_006711832.1:p.Asp898Val
XM_006711770.1:c.1757A>T	XP_006711833.1:p.Asp586Val
XM_011544193.1:c.2504A>T	XP_011542495.1:p.Asp835Val
XM_011544194.1:c.2861A>T	XP_011542496.1:p.Asp954Val
XM_005273141.5:c.2690A>T	XP_005273198.1:p.Asp897Val
XM_006711770.3:c.1757A>T	XP_006711833.1:p.Asp586Val
XM_011544194.3:c.2861A>T	XP_011542496.1:p.Asp954Val
XM_017001329.2:c.2708A>T	XP_016856818.1:p.Asp903Val
XM_017001330.2:c.2672A>T	XP_016856819.1:p.Asp891Val
NM_001291940.2:c.1472A>T	NP_001278869.1:p.Asp491Val
NM_000254.3:c.2693A>T MANE Select	NP_000245.2:p.Asp898Val