Canonical Allele Identifier: CA1140495533

Gene: GALE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23796183C= , CM000663.2:g.23796183C=	GRCh38
NC_000001.10:g.24122673C= , CM000663.1:g.24122673C=	GRCh37
NC_000001.9:g.23995260C=	NCBI36
NG_007068.1:g.9622G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.956G= MANE Select	ENSP00000483375.1:p.Gly319=
ENST00000374497.7:c.956G=	ENSP00000363621.3:p.Gly319=
ENST00000429356.5:c.686G=	ENSP00000398585.1:p.Gly229=
ENST00000456977.5:c.236G=	ENSP00000397045.1:p.Gly79=
ENST00000459934.5:n.1184G=
ENST00000469556.1:n.703G=
ENST00000481736.5:n.1360G=
ENST00000617979.4:c.956G=	ENSP00000483375.1:p.Gly319=
NM_000403.3:c.956G=	NP_000394.2:p.Gly319=
NM_001008216.1:c.956G=	NP_001008217.1:p.Gly319=
NM_001127621.1:c.956G=	NP_001121093.1:p.Gly319=
NM_001008216.2:c.956G= MANE Select	NP_001008217.1:p.Gly319=
NM_000403.4:c.956G=	NP_000394.2:p.Gly319=
NM_001127621.2:c.956G=	NP_001121093.1:p.Gly319=