Canonical Allele Identifier: CA1061922681

Gene: GABRA4

Linked Data

• dbSNP Id: rs1723840753
• gnomAD v3: 4-46993210-GC-G
• gnomAD v4: 4-46993210-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993214del , CM000666.2:g.46993214del	GRCh38
NC_000004.11:g.46995231del , CM000666.1:g.46995231del	GRCh37
NC_000004.10:g.46689988del	NCBI36
NG_011809.1:g.5353del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.86+128del MANE Select	ENSP00000264318.3:n.86+128del
ENST00000264318.3:c.86+128del	ENSP00000264318.3:n.86+128del
ENST00000502874.1:c.86+128del	ENSP00000424386.1:n.86+128del
ENST00000508560.5:c.18+196del	ENSP00000425445.1:n.18+196del
ENST00000509316.1:n.210+128del
ENST00000511523.5:c.18+196del	ENSP00000422152.1:n.18+196del
NM_000809.3:c.86+128del	NP_000800.2:n.86+128del
NM_001204266.1:c.29+196del	NP_001191195.1:n.29+196del
NM_001204267.1:c.29+196del	NP_001191196.1:n.29+196del
XM_011513677.1:c.86+128del	XP_011511979.1:n.86+128del
NM_000809.4:c.86+128del MANE Select	NP_000800.2:n.86+128del
NM_001204266.2:c.29+196del	NP_001191195.1:n.29+196del
NM_001204267.2:c.29+196del	NP_001191196.1:n.29+196del