Canonical Allele Identifier: CA2042508775

Gene: MSRB3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65308634C= , CM000674.2:g.65308634C=	GRCh38
NC_000012.11:g.65702414C= , CM000674.1:g.65702414C=	GRCh37
NC_000012.10:g.63988681C=	NCBI36
NG_023441.1:g.34992C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001031679.3:c.55C= MANE Select	NP_001026849.1:p.Arg19=
ENST00000308259.10:c.55C= MANE Select	ENSP00000312274.6:p.Arg19=
NM_001031679.2:c.55C=	NP_001026849.1:p.Arg19=
NM_001193460.1:c.55C=	NP_001180389.1:p.Arg19=
NM_001193460.2:c.55C=	NP_001180389.1:p.Arg19=
NM_001193461.1:c.55C=	NP_001180390.1:p.Arg19=
NM_001193461.2:c.55C=	NP_001180390.1:p.Arg19=
NM_198080.3:c.98-18192C=	NP_932346.1:n.98-18192C=
NM_198080.4:c.98-18192C=	NP_932346.1:n.98-18192C=
ENST00000308259.9:c.55C=	ENSP00000312274.5:p.Arg19=
ENST00000355192.7:c.98-18192C=	ENSP00000347324.3:n.98-18192C=
ENST00000355192.8:c.98-18192C=	ENSP00000347324.3:n.98-18192C=
ENST00000535239.5:c.55C=	ENSP00000445843.1:p.Arg19=
ENST00000535664.5:c.55C=	ENSP00000441650.1:p.Arg19=
ENST00000538045.5:c.55C=	ENSP00000442620.1:p.Arg19=
ENST00000538725.1:n.268C=
ENST00000540804.5:c.98-18192C=	ENSP00000437623.1:n.98-18192C=
ENST00000541189.5:c.123-18192C=
ENST00000541897.5:c.*68C=	ENSP00000445051.1:n.*68C=
ENST00000614640.4:c.55C=	ENSP00000481483.1:p.Arg19=
ENST00000642404.1:c.55C=	ENSP00000496008.1:p.Arg19=
ENST00000642411.1:c.55C=	ENSP00000494265.1:p.Arg19=
ENST00000645872.1:n.395C=
ENST00000646299.1:c.55C=	ENSP00000494941.1:p.Arg19=
XM_024448918.1:c.55C=	XP_024304686.1:p.Arg19=
XM_024448919.1:c.55C=	XP_024304687.1:p.Arg19=
XM_024448920.1:c.55C=	XP_024304688.1:p.Arg19=
XM_024448921.1:c.55C=	XP_024304689.1:p.Arg19=
XM_024448922.1:c.230-18192C=	XP_024304690.1:n.230-18192C=