Canonical Allele Identifier: CA1158961346

Gene: GALE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23798020_23798021delinsGA , CM000663.2:g.23798020_23798021delinsGA	GRCh38
NC_000001.10:g.24124510_24124511delinsGA , CM000663.1:g.24124510_24124511delinsGA	GRCh37
NC_000001.9:g.23997097_23997098delinsGA	NCBI36
NG_007068.1:g.7784_7785delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.351+96_351+97delinsTC MANE Select	ENSP00000483375.1:n.351+96_351+97delinsTC
ENST00000374497.7:c.351+96_351+97delinsTC	ENSP00000363621.3:n.351+96_351+97delinsTC
ENST00000418277.5:c.159+96_159+97delinsTC	ENSP00000414719.1:n.159+96_159+97delinsTC
ENST00000425913.5:c.351+96_351+97delinsTC	ENSP00000393359.1:n.351+96_351+97delinsTC
ENST00000429356.5:c.159+96_159+97delinsTC	ENSP00000398585.1:n.159+96_159+97delinsTC
ENST00000445705.1:c.351+96_351+97delinsTC	ENSP00000398257.1:n.351+96_351+97delinsTC
ENST00000459934.5:n.469+96_469+97delinsTC
ENST00000467493.5:n.811+96_811+97delinsTC
ENST00000470949.5:n.296+96_296+97delinsTC
ENST00000481736.5:n.755+96_755+97delinsTC
ENST00000617979.4:c.351+96_351+97delinsTC	ENSP00000483375.1:n.351+96_351+97delinsTC
NM_000403.3:c.351+96_351+97delinsTC	NP_000394.2:n.351+96_351+97delinsTC
NM_001008216.1:c.351+96_351+97delinsTC	NP_001008217.1:n.351+96_351+97delinsTC
NM_001127621.1:c.351+96_351+97delinsTC	NP_001121093.1:n.351+96_351+97delinsTC
NM_001008216.2:c.351+96_351+97delinsTC MANE Select	NP_001008217.1:n.351+96_351+97delinsTC
NM_000403.4:c.351+96_351+97delinsTC	NP_000394.2:n.351+96_351+97delinsTC
NM_001127621.2:c.351+96_351+97delinsTC	NP_001121093.1:n.351+96_351+97delinsTC