Canonical Allele Identifier: CA1158961333
Gene: GALE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23797989_23797991delinsCTG , CM000663.2:g.23797989_23797991delinsCTG GRCh38
NC_000001.10:g.24124479_24124481delinsCTG , CM000663.1:g.24124479_24124481delinsCTG GRCh37
NC_000001.9:g.23997066_23997068delinsCTG NCBI36
NG_007068.1:g.7814_7816delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000617979.5:c.352-120_352-118delinsCAG MANE Select ENSP00000483375.1:n.352-120_352-118delinsCAG
ENST00000374497.7:c.352-120_352-118delinsCAG ENSP00000363621.3:n.352-120_352-118delinsCAG
ENST00000418277.5:c.160-120_160-118delinsCAG ENSP00000414719.1:n.160-120_160-118delinsCAG
ENST00000425913.5:c.352-120_352-118delinsCAG ENSP00000393359.1:n.352-120_352-118delinsCAG
ENST00000429356.5:c.160-120_160-118delinsCAG ENSP00000398585.1:n.160-120_160-118delinsCAG
ENST00000445705.1:c.352-120_352-118delinsCAG ENSP00000398257.1:n.352-120_352-118delinsCAG
ENST00000459934.5:n.470-120_470-118delinsCAG
ENST00000467493.5:n.812-120_812-118delinsCAG
ENST00000470949.5:n.297-120_297-118delinsCAG
ENST00000481736.5:n.756-120_756-118delinsCAG
ENST00000617979.4:c.352-120_352-118delinsCAG ENSP00000483375.1:n.352-120_352-118delinsCAG
NM_000403.3:c.352-120_352-118delinsCAG NP_000394.2:n.352-120_352-118delinsCAG
NM_001008216.1:c.352-120_352-118delinsCAG NP_001008217.1:n.352-120_352-118delinsCAG
NM_001127621.1:c.352-120_352-118delinsCAG NP_001121093.1:n.352-120_352-118delinsCAG
NM_001008216.2:c.352-120_352-118delinsCAG MANE Select NP_001008217.1:n.352-120_352-118delinsCAG
NM_000403.4:c.352-120_352-118delinsCAG NP_000394.2:n.352-120_352-118delinsCAG
NM_001127621.2:c.352-120_352-118delinsCAG NP_001121093.1:n.352-120_352-118delinsCAG