Canonical Allele Identifier: CA1158961568

Gene: GALE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23798455C= , CM000663.2:g.23798455C=	GRCh38
NC_000001.10:g.24124945C= , CM000663.1:g.24124945C=	GRCh37
NC_000001.9:g.23997532C=	NCBI36
NG_007068.1:g.7350G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.237+160G= MANE Select	ENSP00000483375.1:n.237+160G=
ENST00000374497.7:c.237+160G=	ENSP00000363621.3:n.237+160G=
ENST00000418277.5:c.45+160G=	ENSP00000414719.1:n.45+160G=
ENST00000425913.5:c.237+160G=	ENSP00000393359.1:n.237+160G=
ENST00000429356.5:c.45+160G=	ENSP00000398585.1:n.45+160G=
ENST00000445705.1:c.237+160G=	ENSP00000398257.1:n.237+160G=
ENST00000459934.5:n.355+160G=
ENST00000466250.5:n.523G=
ENST00000467493.5:n.473G=
ENST00000470383.1:n.1945G=
ENST00000470949.5:n.187+160G=
ENST00000481736.5:n.417G=
ENST00000486382.1:n.343+160G=
ENST00000617979.4:c.237+160G=	ENSP00000483375.1:n.237+160G=
NM_000403.3:c.237+160G=	NP_000394.2:n.237+160G=
NM_001008216.1:c.237+160G=	NP_001008217.1:n.237+160G=
NM_001127621.1:c.237+160G=	NP_001121093.1:n.237+160G=
NM_001008216.2:c.237+160G= MANE Select	NP_001008217.1:n.237+160G=
NM_000403.4:c.237+160G=	NP_000394.2:n.237+160G=
NM_001127621.2:c.237+160G=	NP_001121093.1:n.237+160G=