Canonical Allele Identifier: CA1140495534
Gene: GALE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23796722T= , CM000663.2:g.23796722T= GRCh38
NC_000001.10:g.24123212T= , CM000663.1:g.24123212T= GRCh37
NC_000001.9:g.23995799T= NCBI36
NG_007068.1:g.9083A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617979.5:c.770A= MANE Select ENSP00000483375.1:p.Lys257=
ENST00000374497.7:c.770A= ENSP00000363621.3:p.Lys257=
ENST00000418277.5:c.578A= ENSP00000414719.1:p.Lys193=
ENST00000429356.5:c.578A= ENSP00000398585.1:p.Lys193=
ENST00000456977.5:c.128A= ENSP00000397045.1:p.Lys43=
ENST00000459934.5:n.888A=
ENST00000469556.1:n.164A=
ENST00000481736.5:n.1174A=
ENST00000617979.4:c.770A= ENSP00000483375.1:p.Lys257=
NM_000403.3:c.770A= NP_000394.2:p.Lys257=
NM_001008216.1:c.770A= NP_001008217.1:p.Lys257=
NM_001127621.1:c.770A= NP_001121093.1:p.Lys257=
NM_001008216.2:c.770A= MANE Select NP_001008217.1:p.Lys257=
NM_000403.4:c.770A= NP_000394.2:p.Lys257=
NM_001127621.2:c.770A= NP_001121093.1:p.Lys257=