Canonical Allele Identifier: CA12909947

Gene: MSR1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16177793T>A , CM000670.2:g.16177793T>A	GRCh38
NC_000008.10:g.16035302T>A , CM000670.1:g.16035302T>A	GRCh37
NC_000008.9:g.16079673T>A	NCBI36
NG_012102.1:g.19999A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262101.10:c.103+93A>T MANE Select	ENSP00000262101.5:n.103+93A>T
ENST00000262101.9:c.103+93A>T	ENSP00000262101.5:n.103+93A>T
ENST00000350896.3:c.103+93A>T	ENSP00000262100.3:n.103+93A>T
ENST00000355282.6:c.103+93A>T	ENSP00000347430.2:n.103+93A>T
ENST00000381998.8:c.103+93A>T	ENSP00000371428.4:n.103+93A>T
ENST00000445506.6:c.157+93A>T	ENSP00000405453.2:n.157+93A>T
ENST00000518026.5:c.136+93A>T	ENSP00000429498.1:n.136+93A>T
ENST00000518960.5:c.103+93A>T	ENSP00000427905.1:n.103+93A>T
ENST00000519060.6:c.103+93A>T	ENSP00000428865.1:n.103+93A>T
NM_002445.3:c.103+93A>T	NP_002436.1:n.103+93A>T
NM_138715.2:c.103+93A>T	NP_619729.1:n.103+93A>T
NM_138716.2:c.103+93A>T	NP_619730.1:n.103+93A>T
NM_001363744.1:c.157+93A>T	NP_001350673.1:n.157+93A>T
XM_024447161.1:c.157+93A>T	XP_024302929.1:n.157+93A>T
NM_138715.3:c.103+93A>T MANE Select	NP_619729.1:n.103+93A>T
NM_002445.4:c.103+93A>T	NP_002436.1:n.103+93A>T
NM_138716.3:c.103+93A>T	NP_619730.1:n.103+93A>T