Canonical Allele Identifier: CA1455119188

Gene: GABRA4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993380_46993383delinsCCCG , CM000666.2:g.46993380_46993383delinsCCCG	GRCh38
NC_000004.11:g.46995397_46995400delinsCCCG , CM000666.1:g.46995397_46995400delinsCCCG	GRCh37
NC_000004.10:g.46690154_46690157delinsCCCG	NCBI36
NG_011809.1:g.5181_5184delinsCGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.42_45delinsCGGG MANE Select	ENSP00000264318.3:p.Ala14=
ENST00000264318.3:c.42_45delinsCGGG	ENSP00000264318.3:p.Ala14=
ENST00000502874.1:c.42_45delinsCGGG	ENSP00000424386.1:p.Ala14=
ENST00000508560.5:c.18+24_18+27delinsCGGG	ENSP00000425445.1:n.18+24_18+27delinsCGGG
ENST00000509316.1:n.166_169delinsCGGG
ENST00000511523.5:c.18+24_18+27delinsCGGG	ENSP00000422152.1:n.18+24_18+27delinsCGGG
NM_000809.3:c.42_45delinsCGGG	NP_000800.2:p.Ala14=
NM_001204266.1:c.29+24_29+27delinsCGGG	NP_001191195.1:n.29+24_29+27delinsCGGG
NM_001204267.1:c.29+24_29+27delinsCGGG	NP_001191196.1:n.29+24_29+27delinsCGGG
XM_011513677.1:c.42_45delinsCGGG	XP_011511979.1:p.Ala14=
NM_000809.4:c.42_45delinsCGGG MANE Select	NP_000800.2:p.Ala14=
NM_001204266.2:c.29+24_29+27delinsCGGG	NP_001191195.1:n.29+24_29+27delinsCGGG
NM_001204267.2:c.29+24_29+27delinsCGGG	NP_001191196.1:n.29+24_29+27delinsCGGG