Canonical Allele Identifier: CA1455119095

Gene: GABRA4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993210_46993211delinsGC , CM000666.2:g.46993210_46993211delinsGC	GRCh38
NC_000004.11:g.46995227_46995228delinsGC , CM000666.1:g.46995227_46995228delinsGC	GRCh37
NC_000004.10:g.46689984_46689985delinsGC	NCBI36
NG_011809.1:g.5353_5354delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.86+128_86+129delinsGC MANE Select	ENSP00000264318.3:n.86+128_86+129delinsGC
ENST00000264318.3:c.86+128_86+129delinsGC	ENSP00000264318.3:n.86+128_86+129delinsGC
ENST00000502874.1:c.86+128_86+129delinsGC	ENSP00000424386.1:n.86+128_86+129delinsGC
ENST00000508560.5:c.18+196_18+197delinsGC	ENSP00000425445.1:n.18+196_18+197delinsGC
ENST00000509316.1:n.210+128_210+129delinsGC
ENST00000511523.5:c.18+196_18+197delinsGC	ENSP00000422152.1:n.18+196_18+197delinsGC
NM_000809.3:c.86+128_86+129delinsGC	NP_000800.2:n.86+128_86+129delinsGC
NM_001204266.1:c.29+196_29+197delinsGC	NP_001191195.1:n.29+196_29+197delinsGC
NM_001204267.1:c.29+196_29+197delinsGC	NP_001191196.1:n.29+196_29+197delinsGC
XM_011513677.1:c.86+128_86+129delinsGC	XP_011511979.1:n.86+128_86+129delinsGC
NM_000809.4:c.86+128_86+129delinsGC MANE Select	NP_000800.2:n.86+128_86+129delinsGC
NM_001204266.2:c.29+196_29+197delinsGC	NP_001191195.1:n.29+196_29+197delinsGC
NM_001204267.2:c.29+196_29+197delinsGC	NP_001191196.1:n.29+196_29+197delinsGC