Canonical Allele Identifier: CA1158961350
Gene: GALE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23798024_23798027delinsATAC , CM000663.2:g.23798024_23798027delinsATAC GRCh38
NC_000001.10:g.24124514_24124517delinsATAC , CM000663.1:g.24124514_24124517delinsATAC GRCh37
NC_000001.9:g.23997101_23997104delinsATAC NCBI36
NG_007068.1:g.7778_7781delinsGTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000617979.5:c.351+90_351+93delinsGTAT MANE Select ENSP00000483375.1:n.351+90_351+93delinsGTAT
ENST00000374497.7:c.351+90_351+93delinsGTAT ENSP00000363621.3:n.351+90_351+93delinsGTAT
ENST00000418277.5:c.159+90_159+93delinsGTAT ENSP00000414719.1:n.159+90_159+93delinsGTAT
ENST00000425913.5:c.351+90_351+93delinsGTAT ENSP00000393359.1:n.351+90_351+93delinsGTAT
ENST00000429356.5:c.159+90_159+93delinsGTAT ENSP00000398585.1:n.159+90_159+93delinsGTAT
ENST00000445705.1:c.351+90_351+93delinsGTAT ENSP00000398257.1:n.351+90_351+93delinsGTAT
ENST00000459934.5:n.469+90_469+93delinsGTAT
ENST00000467493.5:n.811+90_811+93delinsGTAT
ENST00000470949.5:n.296+90_296+93delinsGTAT
ENST00000481736.5:n.755+90_755+93delinsGTAT
ENST00000617979.4:c.351+90_351+93delinsGTAT ENSP00000483375.1:n.351+90_351+93delinsGTAT
NM_000403.3:c.351+90_351+93delinsGTAT NP_000394.2:n.351+90_351+93delinsGTAT
NM_001008216.1:c.351+90_351+93delinsGTAT NP_001008217.1:n.351+90_351+93delinsGTAT
NM_001127621.1:c.351+90_351+93delinsGTAT NP_001121093.1:n.351+90_351+93delinsGTAT
NM_001008216.2:c.351+90_351+93delinsGTAT MANE Select NP_001008217.1:n.351+90_351+93delinsGTAT
NM_000403.4:c.351+90_351+93delinsGTAT NP_000394.2:n.351+90_351+93delinsGTAT
NM_001127621.2:c.351+90_351+93delinsGTAT NP_001121093.1:n.351+90_351+93delinsGTAT