Canonical Allele Identifier: CA2487103724

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885214C= , CM000663.2:g.236885214C=	GRCh38
NC_000001.10:g.237048514C= , CM000663.1:g.237048514C=	GRCh37
NC_000001.9:g.235115137C=	NCBI36
NG_008959.1:g.94934C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.2770C= MANE Select	ENSP00000355536.5:p.Leu924=
ENST00000535889.6:c.2617C=	ENSP00000441845.1:p.Leu873=
ENST00000650888.1:c.*1812C=	ENSP00000498393.1:n.*1812C=
ENST00000651455.1:c.*1514C=	ENSP00000498963.1:n.*1514C=
ENST00000674797.2:c.2422C=	ENSP00000502299.2:p.Leu808=
ENST00000679569.1:n.3084C=
ENST00000679842.1:c.2581C=	ENSP00000506109.1:p.Leu861=
ENST00000680454.1:n.3214C=
ENST00000681102.1:c.2590C=	ENSP00000505600.1:p.Leu864=
ENST00000681177.1:c.2332C=	ENSP00000506327.1:p.Leu778=
ENST00000681937.1:n.2964C=
ENST00000366576.3:c.1432C=	ENSP00000355535.3:p.Leu478=
ENST00000366577.9:c.2770C=	ENSP00000355536.5:p.Leu924=
ENST00000535889.5:c.2617C=	ENSP00000441845.1:p.Leu873=
NM_000254.2:c.2770C=	NP_000245.2:p.Leu924=
NM_001291939.1:c.2617C=	NP_001278868.1:p.Leu873=
NM_001291940.1:c.1549C=	NP_001278869.1:p.Leu517=
XM_005273141.3:c.2767C=	XP_005273198.1:p.Leu923=
XM_006711769.2:c.2770C=	XP_006711832.1:p.Leu924=
XM_006711770.1:c.1834C=	XP_006711833.1:p.Leu612=
XM_011544193.1:c.2581C=	XP_011542495.1:p.Leu861=
XM_011544194.1:c.2938C=	XP_011542496.1:p.Leu980=
XM_005273141.5:c.2767C=	XP_005273198.1:p.Leu923=
XM_006711770.3:c.1834C=	XP_006711833.1:p.Leu612=
XM_011544194.3:c.2938C=	XP_011542496.1:p.Leu980=
XM_017001329.2:c.2785C=	XP_016856818.1:p.Leu929=
XM_017001330.2:c.2749C=	XP_016856819.1:p.Leu917=
NM_001291940.2:c.1549C=	NP_001278869.1:p.Leu517=
NM_000254.3:c.2770C= MANE Select	NP_000245.2:p.Leu924=