Canonical Allele Identifier: CA1143663263

Gene: GALE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23798201C= , CM000663.2:g.23798201C=	GRCh38
NC_000001.10:g.24124691C= , CM000663.1:g.24124691C=	GRCh37
NC_000001.9:g.23997278C=	NCBI36
NG_007068.1:g.7604G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.267G= MANE Select	ENSP00000483375.1:p.Ala89=
ENST00000374497.7:c.267G=	ENSP00000363621.3:p.Ala89=
ENST00000418277.5:c.75G=	ENSP00000414719.1:p.Ala25=
ENST00000425913.5:c.267G=	ENSP00000393359.1:p.Ala89=
ENST00000429356.5:c.75G=	ENSP00000398585.1:p.Ala25=
ENST00000445705.1:c.267G=	ENSP00000398257.1:p.Ala89=
ENST00000459934.5:n.385G=
ENST00000467493.5:n.727G=
ENST00000470949.5:n.212G=
ENST00000481736.5:n.671G=
ENST00000486382.1:n.368G=
ENST00000617979.4:c.267G=	ENSP00000483375.1:p.Ala89=
NM_000403.3:c.267G=	NP_000394.2:p.Ala89=
NM_001008216.1:c.267G=	NP_001008217.1:p.Ala89=
NM_001127621.1:c.267G=	NP_001121093.1:p.Ala89=
NM_001008216.2:c.267G= MANE Select	NP_001008217.1:p.Ala89=
NM_000403.4:c.267G=	NP_000394.2:p.Ala89=
NM_001127621.2:c.267G=	NP_001121093.1:p.Ala89=