Canonical Allele Identifier: CA1061922683

Gene: GABRA4

Linked Data

• dbSNP Id: rs1723841670
• gnomAD v3: 4-46993232-TAAG-T
• gnomAD v4: 4-46993232-TAAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993237_46993239del , CM000666.2:g.46993237_46993239del	GRCh38
NC_000004.11:g.46995254_46995256del , CM000666.1:g.46995254_46995256del	GRCh37
NC_000004.10:g.46690011_46690013del	NCBI36
NG_011809.1:g.5329_5331del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.86+104_86+106del MANE Select	ENSP00000264318.3:n.86+104_86+106del
ENST00000264318.3:c.86+104_86+106del	ENSP00000264318.3:n.86+104_86+106del
ENST00000502874.1:c.86+104_86+106del	ENSP00000424386.1:n.86+104_86+106del
ENST00000508560.5:c.18+172_18+174del	ENSP00000425445.1:n.18+172_18+174del
ENST00000509316.1:n.210+104_210+106del
ENST00000511523.5:c.18+172_18+174del	ENSP00000422152.1:n.18+172_18+174del
NM_000809.3:c.86+104_86+106del	NP_000800.2:n.86+104_86+106del
NM_001204266.1:c.29+172_29+174del	NP_001191195.1:n.29+172_29+174del
NM_001204267.1:c.29+172_29+174del	NP_001191196.1:n.29+172_29+174del
XM_011513677.1:c.86+104_86+106del	XP_011511979.1:n.86+104_86+106del
NM_000809.4:c.86+104_86+106del MANE Select	NP_000800.2:n.86+104_86+106del
NM_001204266.2:c.29+172_29+174del	NP_001191195.1:n.29+172_29+174del
NM_001204267.2:c.29+172_29+174del	NP_001191196.1:n.29+172_29+174del