Canonical Allele Identifier: CA1158961385
Gene: GALE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23798104C= , CM000663.2:g.23798104C= GRCh38
NC_000001.10:g.24124594C= , CM000663.1:g.24124594C= GRCh37
NC_000001.9:g.23997181C= NCBI36
NG_007068.1:g.7701G=

Transcript Alleles

HGVS Amino-acid change
ENST00000617979.5:c.351+13G= MANE Select ENSP00000483375.1:n.351+13G=
ENST00000374497.7:c.351+13G= ENSP00000363621.3:n.351+13G=
ENST00000418277.5:c.159+13G= ENSP00000414719.1:n.159+13G=
ENST00000425913.5:c.351+13G= ENSP00000393359.1:n.351+13G=
ENST00000429356.5:c.159+13G= ENSP00000398585.1:n.159+13G=
ENST00000445705.1:c.351+13G= ENSP00000398257.1:n.351+13G=
ENST00000459934.5:n.469+13G=
ENST00000467493.5:n.811+13G=
ENST00000470949.5:n.296+13G=
ENST00000481736.5:n.755+13G=
ENST00000617979.4:c.351+13G= ENSP00000483375.1:n.351+13G=
NM_000403.3:c.351+13G= NP_000394.2:n.351+13G=
NM_001008216.1:c.351+13G= NP_001008217.1:n.351+13G=
NM_001127621.1:c.351+13G= NP_001121093.1:n.351+13G=
NM_001008216.2:c.351+13G= MANE Select NP_001008217.1:n.351+13G=
NM_000403.4:c.351+13G= NP_000394.2:n.351+13G=
NM_001127621.2:c.351+13G= NP_001121093.1:n.351+13G=