Canonical Allele Identifier: CA1158961402

Gene: GALE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23798148_23798150delinsACT , CM000663.2:g.23798148_23798150delinsACT	GRCh38
NC_000001.10:g.24124638_24124640delinsACT , CM000663.1:g.24124638_24124640delinsACT	GRCh37
NC_000001.9:g.23997225_23997227delinsACT	NCBI36
NG_007068.1:g.7655_7657delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.318_320delinsAGT MANE Select	ENSP00000483375.1:p.Arg106=
ENST00000374497.7:c.318_320delinsAGT	ENSP00000363621.3:p.Arg106=
ENST00000418277.5:c.126_128delinsAGT	ENSP00000414719.1:p.Arg42=
ENST00000425913.5:c.318_320delinsAGT	ENSP00000393359.1:p.Arg106=
ENST00000429356.5:c.126_128delinsAGT	ENSP00000398585.1:p.Arg42=
ENST00000445705.1:c.318_320delinsAGT	ENSP00000398257.1:p.Arg106=
ENST00000459934.5:n.436_438delinsAGT
ENST00000467493.5:n.778_780delinsAGT
ENST00000470949.5:n.263_265delinsAGT
ENST00000481736.5:n.722_724delinsAGT
ENST00000486382.1:n.419_421delinsAGT
ENST00000617979.4:c.318_320delinsAGT	ENSP00000483375.1:p.Arg106=
NM_000403.3:c.318_320delinsAGT	NP_000394.2:p.Arg106=
NM_001008216.1:c.318_320delinsAGT	NP_001008217.1:p.Arg106=
NM_001127621.1:c.318_320delinsAGT	NP_001121093.1:p.Arg106=
NM_001008216.2:c.318_320delinsAGT MANE Select	NP_001008217.1:p.Arg106=
NM_000403.4:c.318_320delinsAGT	NP_000394.2:p.Arg106=
NM_001127621.2:c.318_320delinsAGT	NP_001121093.1:p.Arg106=