Canonical Allele Identifier: CA370391513

Gene: MSR1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16168568C>T , CM000670.2:g.16168568C>T	GRCh38
NC_000008.10:g.16026077C>T , CM000670.1:g.16026077C>T	GRCh37
NC_000008.9:g.16070448C>T	NCBI36
NG_012102.1:g.29224G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262101.10:c.520G>A MANE Select	ENSP00000262101.5:p.Asp174Asn
ENST00000262101.9:c.520G>A	ENSP00000262101.5:p.Asp174Asn
ENST00000350896.3:c.520G>A	ENSP00000262100.3:p.Asp174Asn
ENST00000355282.6:c.520G>A	ENSP00000347430.2:p.Asp174Asn
ENST00000381998.8:c.520G>A	ENSP00000371428.4:p.Asp174Asn
ENST00000445506.6:c.574G>A	ENSP00000405453.2:p.Asp192Asn
ENST00000519060.6:c.104-4317G>A	ENSP00000428865.1:n.104-4317G>A
NM_002445.3:c.520G>A	NP_002436.1:p.Asp174Asn
NM_138715.2:c.520G>A	NP_619729.1:p.Asp174Asn
NM_138716.2:c.520G>A	NP_619730.1:p.Asp174Asn
NM_001363744.1:c.574G>A	NP_001350673.1:p.Asp192Asn
XM_024447161.1:c.574G>A	XP_024302929.1:p.Asp192Asn
NM_138715.3:c.520G>A MANE Select	NP_619729.1:p.Asp174Asn
NM_002445.4:c.520G>A	NP_002436.1:p.Asp174Asn
NM_138716.3:c.520G>A	NP_619730.1:p.Asp174Asn