Canonical Allele Identifier: CA1141580669

Gene: GALE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23796234C= , CM000663.2:g.23796234C=	GRCh38
NC_000001.10:g.24122724C= , CM000663.1:g.24122724C=	GRCh37
NC_000001.9:g.23995311C=	NCBI36
NG_007068.1:g.9571G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001008216.2:c.905G= MANE Select	NP_001008217.1:p.Gly302=
ENST00000617979.5:c.905G= MANE Select	ENSP00000483375.1:p.Gly302=
NM_000403.3:c.905G=	NP_000394.2:p.Gly302=
NM_000403.4:c.905G=	NP_000394.2:p.Gly302=
NM_001008216.1:c.905G=	NP_001008217.1:p.Gly302=
NM_001127621.1:c.905G=	NP_001121093.1:p.Gly302=
NM_001127621.2:c.905G=	NP_001121093.1:p.Gly302=
ENST00000374497.7:c.905G=	ENSP00000363621.3:p.Gly302=
ENST00000429356.5:c.635G=	ENSP00000398585.1:p.Gly212=
ENST00000456977.5:c.185G=	ENSP00000397045.1:p.Gly62=
ENST00000459934.5:n.1133G=
ENST00000469556.1:n.652G=
ENST00000481736.5:n.1309G=
ENST00000617979.4:c.905G=	ENSP00000483375.1:p.Gly302=