Canonical Allele Identifier: CA2761311578

Gene: GABRA4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993197_46993198dup , CM000666.2:g.46993197_46993198dup	GRCh38
NC_000004.11:g.46995214_46995215dup , CM000666.1:g.46995214_46995215dup	GRCh37
NC_000004.10:g.46689971_46689972dup	NCBI36
NG_011809.1:g.5368_5369dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.86+143_86+144dup MANE Select	ENSP00000264318.3:n.86+143_86+144dup
ENST00000264318.3:c.86+143_86+144dup	ENSP00000264318.3:n.86+143_86+144dup
ENST00000502874.1:c.86+143_86+144dup	ENSP00000424386.1:n.86+143_86+144dup
ENST00000508560.5:c.18+211_18+212dup	ENSP00000425445.1:n.18+211_18+212dup
ENST00000509316.1:n.210+143_210+144dup
ENST00000511523.5:c.18+211_18+212dup	ENSP00000422152.1:n.18+211_18+212dup
NM_000809.3:c.86+143_86+144dup	NP_000800.2:n.86+143_86+144dup
NM_001204266.1:c.29+211_29+212dup	NP_001191195.1:n.29+211_29+212dup
NM_001204267.1:c.29+211_29+212dup	NP_001191196.1:n.29+211_29+212dup
XM_011513677.1:c.86+143_86+144dup	XP_011511979.1:n.86+143_86+144dup
NM_000809.4:c.86+143_86+144dup MANE Select	NP_000800.2:n.86+143_86+144dup
NM_001204266.2:c.29+211_29+212dup	NP_001191195.1:n.29+211_29+212dup
NM_001204267.2:c.29+211_29+212dup	NP_001191196.1:n.29+211_29+212dup