Canonical Allele Identifier: CA439168569

Gene: GABRA4

Linked Data

• MyVariant Identifiers: chr4:g.46995385G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993368G>C , CM000666.2:g.46993368G>C	GRCh38
NC_000004.11:g.46995385G>C , CM000666.1:g.46995385G>C	GRCh37
NC_000004.10:g.46690142G>C	NCBI36
NG_011809.1:g.5196C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.57C>G MANE Select	ENSP00000264318.3:p.Ala19=
ENST00000264318.3:c.57C>G	ENSP00000264318.3:p.Ala19=
ENST00000502874.1:c.57C>G	ENSP00000424386.1:p.Ala19=
ENST00000508560.5:c.18+39C>G	ENSP00000425445.1:n.18+39C>G
ENST00000509316.1:n.181C>G
ENST00000511523.5:c.18+39C>G	ENSP00000422152.1:n.18+39C>G
NM_000809.3:c.57C>G	NP_000800.2:p.Ala19=
NM_001204266.1:c.29+39C>G	NP_001191195.1:n.29+39C>G
NM_001204267.1:c.29+39C>G	NP_001191196.1:n.29+39C>G
XM_011513677.1:c.57C>G	XP_011511979.1:p.Ala19=
NM_000809.4:c.57C>G MANE Select	NP_000800.2:p.Ala19=
NM_001204266.2:c.29+39C>G	NP_001191195.1:n.29+39C>G
NM_001204267.2:c.29+39C>G	NP_001191196.1:n.29+39C>G