Canonical Allele Identifier: CA1158961589

Gene: GALE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23798506G= , CM000663.2:g.23798506G=	GRCh38
NC_000001.10:g.24124996G= , CM000663.1:g.24124996G=	GRCh37
NC_000001.9:g.23997583G=	NCBI36
NG_007068.1:g.7299C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.237+109C= MANE Select	ENSP00000483375.1:n.237+109C=
ENST00000374497.7:c.237+109C=	ENSP00000363621.3:n.237+109C=
ENST00000418277.5:c.45+109C=	ENSP00000414719.1:n.45+109C=
ENST00000425913.5:c.237+109C=	ENSP00000393359.1:n.237+109C=
ENST00000429356.5:c.45+109C=	ENSP00000398585.1:n.45+109C=
ENST00000445705.1:c.237+109C=	ENSP00000398257.1:n.237+109C=
ENST00000459934.5:n.355+109C=
ENST00000466250.5:n.472C=
ENST00000467493.5:n.422C=
ENST00000470383.1:n.1894C=
ENST00000470949.5:n.187+109C=
ENST00000481736.5:n.366C=
ENST00000486382.1:n.343+109C=
ENST00000617979.4:c.237+109C=	ENSP00000483375.1:n.237+109C=
NM_000403.3:c.237+109C=	NP_000394.2:n.237+109C=
NM_001008216.1:c.237+109C=	NP_001008217.1:n.237+109C=
NM_001127621.1:c.237+109C=	NP_001121093.1:n.237+109C=
NM_001008216.2:c.237+109C= MANE Select	NP_001008217.1:n.237+109C=
NM_000403.4:c.237+109C=	NP_000394.2:n.237+109C=
NM_001127621.2:c.237+109C=	NP_001121093.1:n.237+109C=