Canonical Allele Identifier: CA1766885887

Gene: MSR1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16155201G= , CM000670.2:g.16155201G=	GRCh38
NC_000008.10:g.16012710G= , CM000670.1:g.16012710G=	GRCh37
NC_000008.9:g.16057081G=	NCBI36
NG_012102.1:g.42591C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262101.10:c.818-57C= MANE Select	ENSP00000262101.5:n.818-57C=
ENST00000262101.9:c.818-57C=	ENSP00000262101.5:n.818-57C=
ENST00000350896.3:c.818-57C=	ENSP00000262100.3:n.818-57C=
ENST00000355282.6:c.818-57C=	ENSP00000347430.2:n.818-57C=
ENST00000381998.8:c.818-57C=	ENSP00000371428.4:n.818-57C=
ENST00000445506.6:c.872-57C=	ENSP00000405453.2:n.872-57C=
ENST00000519060.6:c.*177-57C=	ENSP00000428865.1:n.*177-57C=
ENST00000522672.5:c.188-57C=	ENSP00000430536.1:n.188-57C=
NM_002445.3:c.818-57C=	NP_002436.1:n.818-57C=
NM_138715.2:c.818-57C=	NP_619729.1:n.818-57C=
NM_138716.2:c.818-57C=	NP_619730.1:n.818-57C=
NM_001363744.1:c.872-57C=	NP_001350673.1:n.872-57C=
XM_024447161.1:c.872-57C=	XP_024302929.1:n.872-57C=
NM_138715.3:c.818-57C= MANE Select	NP_619729.1:n.818-57C=
NM_002445.4:c.818-57C=	NP_002436.1:n.818-57C=
NM_138716.3:c.818-57C=	NP_619730.1:n.818-57C=