Canonical Allele Identifier: CA1455119026

Gene: GABRA4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993115_46993116delinsGC , CM000666.2:g.46993115_46993116delinsGC	GRCh38
NC_000004.11:g.46995132_46995133delinsGC , CM000666.1:g.46995132_46995133delinsGC	GRCh37
NC_000004.10:g.46689889_46689890delinsGC	NCBI36
NG_011809.1:g.5448_5449delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.87-170_87-169delinsGC MANE Select	ENSP00000264318.3:n.87-170_87-169delinsGC
ENST00000264318.3:c.87-170_87-169delinsGC	ENSP00000264318.3:n.87-170_87-169delinsGC
ENST00000502874.1:c.86+223_86+224delinsGC	ENSP00000424386.1:n.86+223_86+224delinsGC
ENST00000508560.5:c.19-170_19-169delinsGC	ENSP00000425445.1:n.19-170_19-169delinsGC
ENST00000509316.1:n.211-170_211-169delinsGC
ENST00000511523.5:c.19-170_19-169delinsGC	ENSP00000422152.1:n.19-170_19-169delinsGC
NM_000809.3:c.87-170_87-169delinsGC	NP_000800.2:n.87-170_87-169delinsGC
NM_001204266.1:c.30-170_30-169delinsGC	NP_001191195.1:n.30-170_30-169delinsGC
NM_001204267.1:c.30-170_30-169delinsGC	NP_001191196.1:n.30-170_30-169delinsGC
XM_011513677.1:c.87-170_87-169delinsGC	XP_011511979.1:n.87-170_87-169delinsGC
NM_000809.4:c.87-170_87-169delinsGC MANE Select	NP_000800.2:n.87-170_87-169delinsGC
NM_001204266.2:c.30-170_30-169delinsGC	NP_001191195.1:n.30-170_30-169delinsGC
NM_001204267.2:c.30-170_30-169delinsGC	NP_001191196.1:n.30-170_30-169delinsGC