Canonical Allele Identifier: CA1158961590
Gene: GALE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23798508_23798509delinsGT , CM000663.2:g.23798508_23798509delinsGT GRCh38
NC_000001.10:g.24124998_24124999delinsGT , CM000663.1:g.24124998_24124999delinsGT GRCh37
NC_000001.9:g.23997585_23997586delinsGT NCBI36
NG_007068.1:g.7296_7297delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000617979.5:c.237+106_237+107delinsAC MANE Select ENSP00000483375.1:n.237+106_237+107delinsAC
ENST00000374497.7:c.237+106_237+107delinsAC ENSP00000363621.3:n.237+106_237+107delinsAC
ENST00000418277.5:c.45+106_45+107delinsAC ENSP00000414719.1:n.45+106_45+107delinsAC
ENST00000425913.5:c.237+106_237+107delinsAC ENSP00000393359.1:n.237+106_237+107delinsAC
ENST00000429356.5:c.45+106_45+107delinsAC ENSP00000398585.1:n.45+106_45+107delinsAC
ENST00000445705.1:c.237+106_237+107delinsAC ENSP00000398257.1:n.237+106_237+107delinsAC
ENST00000459934.5:n.355+106_355+107delinsAC
ENST00000466250.5:n.469_470delinsAC
ENST00000467493.5:n.419_420delinsAC
ENST00000470383.1:n.1891_1892delinsAC
ENST00000470949.5:n.187+106_187+107delinsAC
ENST00000481736.5:n.363_364delinsAC
ENST00000486382.1:n.343+106_343+107delinsAC
ENST00000617979.4:c.237+106_237+107delinsAC ENSP00000483375.1:n.237+106_237+107delinsAC
NM_000403.3:c.237+106_237+107delinsAC NP_000394.2:n.237+106_237+107delinsAC
NM_001008216.1:c.237+106_237+107delinsAC NP_001008217.1:n.237+106_237+107delinsAC
NM_001127621.1:c.237+106_237+107delinsAC NP_001121093.1:n.237+106_237+107delinsAC
NM_001008216.2:c.237+106_237+107delinsAC MANE Select NP_001008217.1:n.237+106_237+107delinsAC
NM_000403.4:c.237+106_237+107delinsAC NP_000394.2:n.237+106_237+107delinsAC
NM_001127621.2:c.237+106_237+107delinsAC NP_001121093.1:n.237+106_237+107delinsAC