Canonical Allele Identifier: CA2742818860

Gene: GALE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23798366_23798367insAGACTGCAAAAAAAACCCAAACACAC , CM000663.2:g.23798366_23798367insAGACTGCAAAAAAAACCCAAACACAC	GRCh38
NC_000001.10:g.24124856_24124857insAGACTGCAAAAAAAACCCAAACACAC , CM000663.1:g.24124856_24124857insAGACTGCAAAAAAAACCCAAACACAC	GRCh37
NC_000001.9:g.23997443_23997444insAGACTGCAAAAAAAACCCAAACACAC	NCBI36
NG_007068.1:g.7438_7439insGTGTGTTTGGGTTTTTTTTGCAGTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT MANE Select	ENSP00000483375.1:n.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAG...
ENST00000374497.7:c.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT	ENSP00000363621.3:n.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAG...
ENST00000418277.5:c.46-137_46-136insGTGTGTTTGGGTTTTTTTTGCAGTCT	ENSP00000414719.1:n.46-137_46-136insGTGTGTTTGGGTTTTTTTTGCAGTC...
ENST00000425913.5:c.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT	ENSP00000393359.1:n.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAG...
ENST00000429356.5:c.46-137_46-136insGTGTGTTTGGGTTTTTTTTGCAGTCT	ENSP00000398585.1:n.46-137_46-136insGTGTGTTTGGGTTTTTTTTGCAGTC...
ENST00000445705.1:c.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT	ENSP00000398257.1:n.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAG...
ENST00000459934.5:n.356-137_356-136insGTGTGTTTGGGTTTTTTTTGCAGTCT
ENST00000467493.5:n.561_562insGTGTGTTTGGGTTTTTTTTGCAGTCT
ENST00000470383.1:n.2033_2034insGTGTGTTTGGGTTTTTTTTGCAGTCT
ENST00000470949.5:n.188-142_188-141insGTGTGTTTGGGTTTTTTTTGCAGTCT
ENST00000481736.5:n.505_506insGTGTGTTTGGGTTTTTTTTGCAGTCT
ENST00000486382.1:n.344-142_344-141insGTGTGTTTGGGTTTTTTTTGCAGTCT
ENST00000617979.4:c.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT	ENSP00000483375.1:n.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAG...
NM_000403.3:c.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT	NP_000394.2:n.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT
NM_001008216.1:c.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT	NP_001008217.1:n.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT...
NM_001127621.1:c.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT	NP_001121093.1:n.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT...
NM_001008216.2:c.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT MANE Select	NP_001008217.1:n.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT...
NM_000403.4:c.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT	NP_000394.2:n.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT
NM_001127621.2:c.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT	NP_001121093.1:n.238-137_238-136insGTGTGTTTGGGTTTTTTTTGCAGTCT...