Canonical Allele Identifier: CA4641124

Gene: MSR1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16155085G>C , CM000670.2:g.16155085G>C	GRCh38
NC_000008.10:g.16012594G>C , CM000670.1:g.16012594G>C	GRCh37
NC_000008.9:g.16056965G>C	NCBI36
NG_012102.1:g.42707C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262101.10:c.877C>G MANE Select	ENSP00000262101.5:p.Arg293Gly
ENST00000262101.9:c.877C>G	ENSP00000262101.5:p.Arg293Gly
ENST00000350896.3:c.877C>G	ENSP00000262100.3:p.Arg293Gly
ENST00000355282.6:c.877C>G	ENSP00000347430.2:p.Arg293Gly
ENST00000381998.8:c.877C>G	ENSP00000371428.4:p.Arg293Gly
ENST00000445506.6:c.931C>G	ENSP00000405453.2:p.Arg311Gly
ENST00000519060.6:c.*236C>G	ENSP00000428865.1:n.*236C>G
ENST00000522672.5:c.247C>G	ENSP00000430536.1:p.Arg83Gly
NM_002445.3:c.877C>G	NP_002436.1:p.Arg293Gly
NM_138715.2:c.877C>G	NP_619729.1:p.Arg293Gly
NM_138716.2:c.877C>G	NP_619730.1:p.Arg293Gly
NM_001363744.1:c.931C>G	NP_001350673.1:p.Arg311Gly
XM_024447161.1:c.931C>G	XP_024302929.1:p.Arg311Gly
NM_138715.3:c.877C>G MANE Select	NP_619729.1:p.Arg293Gly
NM_002445.4:c.877C>G	NP_002436.1:p.Arg293Gly
NM_138716.3:c.877C>G	NP_619730.1:p.Arg293Gly