Canonical Allele Identifier: CA1158960749

Gene: GALE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23796558T= , CM000663.2:g.23796558T=	GRCh38
NC_000001.10:g.24123048T= , CM000663.1:g.24123048T=	GRCh37
NC_000001.9:g.23995635T=	NCBI36
NG_007068.1:g.9247A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.824A= MANE Select	ENSP00000483375.1:p.Tyr275=
ENST00000374497.7:c.824A=	ENSP00000363621.3:p.Tyr275=
ENST00000418277.5:c.632A=	ENSP00000414719.1:p.Tyr211=
ENST00000429356.5:c.603+139A=	ENSP00000398585.1:n.603+139A=
ENST00000456977.5:c.153+139A=	ENSP00000397045.1:n.153+139A=
ENST00000459934.5:n.1052A=
ENST00000469556.1:n.328A=
ENST00000481736.5:n.1228A=
ENST00000617979.4:c.824A=	ENSP00000483375.1:p.Tyr275=
NM_000403.3:c.824A=	NP_000394.2:p.Tyr275=
NM_001008216.1:c.824A=	NP_001008217.1:p.Tyr275=
NM_001127621.1:c.824A=	NP_001121093.1:p.Tyr275=
NM_001008216.2:c.824A= MANE Select	NP_001008217.1:p.Tyr275=
NM_000403.4:c.824A=	NP_000394.2:p.Tyr275=
NM_001127621.2:c.824A=	NP_001121093.1:p.Tyr275=