Canonical Allele Identifier: CA1158960767

Gene: GALE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23796587C= , CM000663.2:g.23796587C=	GRCh38
NC_000001.10:g.24123077C= , CM000663.1:g.24123077C=	GRCh37
NC_000001.9:g.23995664C=	NCBI36
NG_007068.1:g.9218G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.796-1G= MANE Select	ENSP00000483375.1:n.796-1G=
ENST00000374497.7:c.796-1G=	ENSP00000363621.3:n.796-1G=
ENST00000418277.5:c.604-1G=	ENSP00000414719.1:n.604-1G=
ENST00000429356.5:c.603+110G=	ENSP00000398585.1:n.603+110G=
ENST00000456977.5:c.153+110G=	ENSP00000397045.1:n.153+110G=
ENST00000459934.5:n.1023G=
ENST00000469556.1:n.299G=
ENST00000481736.5:n.1200-1G=
ENST00000617979.4:c.796-1G=	ENSP00000483375.1:n.796-1G=
NM_000403.3:c.796-1G=	NP_000394.2:n.796-1G=
NM_001008216.1:c.796-1G=	NP_001008217.1:n.796-1G=
NM_001127621.1:c.796-1G=	NP_001121093.1:n.796-1G=
NM_001008216.2:c.796-1G= MANE Select	NP_001008217.1:n.796-1G=
NM_000403.4:c.796-1G=	NP_000394.2:n.796-1G=
NM_001127621.2:c.796-1G=	NP_001121093.1:n.796-1G=