Canonical Allele Identifier: CA1158961383
Gene: GALE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23798100T= , CM000663.2:g.23798100T= GRCh38
NC_000001.10:g.24124590T= , CM000663.1:g.24124590T= GRCh37
NC_000001.9:g.23997177T= NCBI36
NG_007068.1:g.7705A=

Transcript Alleles

HGVS Amino-acid change
ENST00000617979.5:c.351+17A= MANE Select ENSP00000483375.1:n.351+17A=
ENST00000374497.7:c.351+17A= ENSP00000363621.3:n.351+17A=
ENST00000418277.5:c.159+17A= ENSP00000414719.1:n.159+17A=
ENST00000425913.5:c.351+17A= ENSP00000393359.1:n.351+17A=
ENST00000429356.5:c.159+17A= ENSP00000398585.1:n.159+17A=
ENST00000445705.1:c.351+17A= ENSP00000398257.1:n.351+17A=
ENST00000459934.5:n.469+17A=
ENST00000467493.5:n.811+17A=
ENST00000470949.5:n.296+17A=
ENST00000481736.5:n.755+17A=
ENST00000617979.4:c.351+17A= ENSP00000483375.1:n.351+17A=
NM_000403.3:c.351+17A= NP_000394.2:n.351+17A=
NM_001008216.1:c.351+17A= NP_001008217.1:n.351+17A=
NM_001127621.1:c.351+17A= NP_001121093.1:n.351+17A=
NM_001008216.2:c.351+17A= MANE Select NP_001008217.1:n.351+17A=
NM_000403.4:c.351+17A= NP_000394.2:n.351+17A=
NM_001127621.2:c.351+17A= NP_001121093.1:n.351+17A=