Canonical Allele Identifier: CA2670526393
Gene: GABRA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46993327del , CM000666.2:g.46993327del GRCh38
NC_000004.11:g.46995344del , CM000666.1:g.46995344del GRCh37
NC_000004.10:g.46690101del NCBI36
NG_011809.1:g.5240del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264318.4:c.86+15del MANE Select ENSP00000264318.3:n.86+15del
ENST00000264318.3:c.86+15del ENSP00000264318.3:n.86+15del
ENST00000502874.1:c.86+15del ENSP00000424386.1:n.86+15del
ENST00000508560.5:c.18+83del ENSP00000425445.1:n.18+83del
ENST00000509316.1:n.210+15del
ENST00000511523.5:c.18+83del ENSP00000422152.1:n.18+83del
NM_000809.3:c.86+15del NP_000800.2:n.86+15del
NM_001204266.1:c.29+83del NP_001191195.1:n.29+83del
NM_001204267.1:c.29+83del NP_001191196.1:n.29+83del
XM_011513677.1:c.86+15del XP_011511979.1:n.86+15del
NM_000809.4:c.86+15del MANE Select NP_000800.2:n.86+15del
NM_001204266.2:c.29+83del NP_001191195.1:n.29+83del
NM_001204267.2:c.29+83del NP_001191196.1:n.29+83del