Canonical Allele Identifier: CA1158961414

Gene: GALE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23798175_23798176delinsAC , CM000663.2:g.23798175_23798176delinsAC	GRCh38
NC_000001.10:g.24124665_24124666delinsAC , CM000663.1:g.24124665_24124666delinsAC	GRCh37
NC_000001.9:g.23997252_23997253delinsAC	NCBI36
NG_007068.1:g.7629_7630delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.292_293delinsGT MANE Select	ENSP00000483375.1:p.Val98=
ENST00000374497.7:c.292_293delinsGT	ENSP00000363621.3:p.Val98=
ENST00000418277.5:c.100_101delinsGT	ENSP00000414719.1:p.Val34=
ENST00000425913.5:c.292_293delinsGT	ENSP00000393359.1:p.Val98=
ENST00000429356.5:c.100_101delinsGT	ENSP00000398585.1:p.Val34=
ENST00000445705.1:c.292_293delinsGT	ENSP00000398257.1:p.Val98=
ENST00000459934.5:n.410_411delinsGT
ENST00000467493.5:n.752_753delinsGT
ENST00000470949.5:n.237_238delinsGT
ENST00000481736.5:n.696_697delinsGT
ENST00000486382.1:n.393_394delinsGT
ENST00000617979.4:c.292_293delinsGT	ENSP00000483375.1:p.Val98=
NM_000403.3:c.292_293delinsGT	NP_000394.2:p.Val98=
NM_001008216.1:c.292_293delinsGT	NP_001008217.1:p.Val98=
NM_001127621.1:c.292_293delinsGT	NP_001121093.1:p.Val98=
NM_001008216.2:c.292_293delinsGT MANE Select	NP_001008217.1:p.Val98=
NM_000403.4:c.292_293delinsGT	NP_000394.2:p.Val98=
NM_001127621.2:c.292_293delinsGT	NP_001121093.1:p.Val98=