Canonical Allele Identifier: CA1766885752

Gene: MSR1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16155139G= , CM000670.2:g.16155139G=	GRCh38
NC_000008.10:g.16012648G= , CM000670.1:g.16012648G=	GRCh37
NC_000008.9:g.16057019G=	NCBI36
NG_012102.1:g.42653C=

Transcript Alleles

HGVS	Amino-acid Change
NM_138715.3:c.823C= MANE Select	NP_619729.1:p.Pro275=
ENST00000262101.10:c.823C= MANE Select	ENSP00000262101.5:p.Pro275=
NM_001363744.1:c.877C=	NP_001350673.1:p.Pro293=
NM_002445.3:c.823C=	NP_002436.1:p.Pro275=
NM_002445.4:c.823C=	NP_002436.1:p.Pro275=
NM_138715.2:c.823C=	NP_619729.1:p.Pro275=
NM_138716.2:c.823C=	NP_619730.1:p.Pro275=
NM_138716.3:c.823C=	NP_619730.1:p.Pro275=
ENST00000262101.9:c.823C=	ENSP00000262101.5:p.Pro275=
ENST00000350896.3:c.823C=	ENSP00000262100.3:p.Pro275=
ENST00000355282.6:c.823C=	ENSP00000347430.2:p.Pro275=
ENST00000381998.8:c.823C=	ENSP00000371428.4:p.Pro275=
ENST00000445506.6:c.877C=	ENSP00000405453.2:p.Pro293=
ENST00000519060.6:c.*182C=	ENSP00000428865.1:n.*182C=
ENST00000522672.5:c.193C=	ENSP00000430536.1:p.Pro65=
XM_024447161.1:c.877C=	XP_024302929.1:p.Pro293=