Canonical Allele Identifier: CA1141580656

Gene: GALE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23797718G= , CM000663.2:g.23797718G=	GRCh38
NC_000001.10:g.24124208G= , CM000663.1:g.24124208G=	GRCh37
NC_000001.9:g.23996795G=	NCBI36
NG_007068.1:g.8087C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001008216.2:c.505C= MANE Select	NP_001008217.1:p.Arg169=
ENST00000617979.5:c.505C= MANE Select	ENSP00000483375.1:p.Arg169=
NM_000403.3:c.505C=	NP_000394.2:p.Arg169=
NM_000403.4:c.505C=	NP_000394.2:p.Arg169=
NM_001008216.1:c.505C=	NP_001008217.1:p.Arg169=
NM_001127621.1:c.505C=	NP_001121093.1:p.Arg169=
NM_001127621.2:c.505C=	NP_001121093.1:p.Arg169=
ENST00000374497.7:c.505C=	ENSP00000363621.3:p.Arg169=
ENST00000418277.5:c.313C=	ENSP00000414719.1:p.Arg105=
ENST00000425913.5:c.505C=	ENSP00000393359.1:p.Arg169=
ENST00000429356.5:c.313C=	ENSP00000398585.1:p.Arg105=
ENST00000445705.1:c.505C=	ENSP00000398257.1:p.Arg169=
ENST00000459934.5:n.623C=
ENST00000467493.5:n.965C=
ENST00000470949.5:n.450C=
ENST00000481736.5:n.909C=
ENST00000617979.4:c.505C=	ENSP00000483375.1:p.Arg169=