Canonical Allele Identifier: CA1455119089

Gene: GABRA4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993202T= , CM000666.2:g.46993202T=	GRCh38
NC_000004.11:g.46995219T= , CM000666.1:g.46995219T=	GRCh37
NC_000004.10:g.46689976T=	NCBI36
NG_011809.1:g.5362A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.86+137A= MANE Select	ENSP00000264318.3:n.86+137A=
ENST00000264318.3:c.86+137A=	ENSP00000264318.3:n.86+137A=
ENST00000502874.1:c.86+137A=	ENSP00000424386.1:n.86+137A=
ENST00000508560.5:c.18+205A=	ENSP00000425445.1:n.18+205A=
ENST00000509316.1:n.210+137A=
ENST00000511523.5:c.18+205A=	ENSP00000422152.1:n.18+205A=
NM_000809.3:c.86+137A=	NP_000800.2:n.86+137A=
NM_001204266.1:c.29+205A=	NP_001191195.1:n.29+205A=
NM_001204267.1:c.29+205A=	NP_001191196.1:n.29+205A=
XM_011513677.1:c.86+137A=	XP_011511979.1:n.86+137A=
NM_000809.4:c.86+137A= MANE Select	NP_000800.2:n.86+137A=
NM_001204266.2:c.29+205A=	NP_001191195.1:n.29+205A=
NM_001204267.2:c.29+205A=	NP_001191196.1:n.29+205A=