Canonical Allele Identifier: CA339007100
Gene: GALE HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000617979.5:c.770A>T MANE Select ENSP00000483375.1:p.Lys257Met
ENST00000374497.7:c.770A>T ENSP00000363621.3:p.Lys257Met
ENST00000418277.5:c.578A>T ENSP00000414719.1:p.Lys193Met
ENST00000429356.5:c.578A>T ENSP00000398585.1:p.Lys193Met
ENST00000456977.5:c.128A>T ENSP00000397045.1:p.Lys43Met
ENST00000459934.5:n.888A>T
ENST00000469556.1:n.164A>T
ENST00000481736.5:n.1174A>T
ENST00000617979.4:c.770A>T ENSP00000483375.1:p.Lys257Met
NM_000403.3:c.770A>T NP_000394.2:p.Lys257Met
NM_001008216.1:c.770A>T NP_001008217.1:p.Lys257Met
NM_001127621.1:c.770A>T NP_001121093.1:p.Lys257Met
NM_001008216.2:c.770A>T MANE Select NP_001008217.1:p.Lys257Met
NM_000403.4:c.770A>T NP_000394.2:p.Lys257Met
NM_001127621.2:c.770A>T NP_001121093.1:p.Lys257Met