Canonical Allele Identifier: CA1158961397

Gene: GALE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23798131T= , CM000663.2:g.23798131T=	GRCh38
NC_000001.10:g.24124621T= , CM000663.1:g.24124621T=	GRCh37
NC_000001.9:g.23997208T=	NCBI36
NG_007068.1:g.7674A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.337A= MANE Select	ENSP00000483375.1:p.Ile113=
ENST00000374497.7:c.337A=	ENSP00000363621.3:p.Ile113=
ENST00000418277.5:c.145A=	ENSP00000414719.1:p.Ile49=
ENST00000425913.5:c.337A=	ENSP00000393359.1:p.Ile113=
ENST00000429356.5:c.145A=	ENSP00000398585.1:p.Ile49=
ENST00000445705.1:c.337A=	ENSP00000398257.1:p.Ile113=
ENST00000459934.5:n.455A=
ENST00000467493.5:n.797A=
ENST00000470949.5:n.282A=
ENST00000481736.5:n.741A=
ENST00000486382.1:n.438A=
ENST00000617979.4:c.337A=	ENSP00000483375.1:p.Ile113=
NM_000403.3:c.337A=	NP_000394.2:p.Ile113=
NM_001008216.1:c.337A=	NP_001008217.1:p.Ile113=
NM_001127621.1:c.337A=	NP_001121093.1:p.Ile113=
NM_001008216.2:c.337A= MANE Select	NP_001008217.1:p.Ile113=
NM_000403.4:c.337A=	NP_000394.2:p.Ile113=
NM_001127621.2:c.337A=	NP_001121093.1:p.Ile113=