Canonical Allele Identifier: CA1158960764
Gene: GALE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23796586T= , CM000663.2:g.23796586T= GRCh38
NC_000001.10:g.24123076T= , CM000663.1:g.24123076T= GRCh37
NC_000001.9:g.23995663T= NCBI36
NG_007068.1:g.9219A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617979.5:c.796A= MANE Select ENSP00000483375.1:p.Ile266=
ENST00000374497.7:c.796A= ENSP00000363621.3:p.Ile266=
ENST00000418277.5:c.604A= ENSP00000414719.1:p.Ile202=
ENST00000429356.5:c.603+111A= ENSP00000398585.1:n.603+111A=
ENST00000456977.5:c.153+111A= ENSP00000397045.1:n.153+111A=
ENST00000459934.5:n.1024A=
ENST00000469556.1:n.300A=
ENST00000481736.5:n.1200A=
ENST00000617979.4:c.796A= ENSP00000483375.1:p.Ile266=
NM_000403.3:c.796A= NP_000394.2:p.Ile266=
NM_001008216.1:c.796A= NP_001008217.1:p.Ile266=
NM_001127621.1:c.796A= NP_001121093.1:p.Ile266=
NM_001008216.2:c.796A= MANE Select NP_001008217.1:p.Ile266=
NM_000403.4:c.796A= NP_000394.2:p.Ile266=
NM_001127621.2:c.796A= NP_001121093.1:p.Ile266=