Canonical Allele Identifier: CA356778095

Gene: GABRA4

Linked Data

• gnomAD v4: 4-46993424-T-C
• MyVariant Identifiers: chr4:g.46995441T>C (hg19) ; chr4:g.46993424T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993424T>C , CM000666.2:g.46993424T>C	GRCh38
NC_000004.11:g.46995441T>C , CM000666.1:g.46995441T>C	GRCh37
NC_000004.10:g.46690198T>C	NCBI36
NG_011809.1:g.5140A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.1A>G MANE Select	ENSP00000264318.3:p.Met1Val
ENST00000264318.3:c.1A>G	ENSP00000264318.3:p.Met1Val
ENST00000502874.1:c.1A>G	ENSP00000424386.1:p.Met1Val
ENST00000508560.5:c.1A>G	ENSP00000425445.1:p.Met1Val
ENST00000509316.1:n.125A>G
ENST00000511523.5:c.1A>G	ENSP00000422152.1:p.Met1Val
NM_000809.3:c.1A>G	NP_000800.2:p.Met1Val
NM_001204266.1:c.12A>G	NP_001191195.1:p.Arg4=
NM_001204267.1:c.12A>G	NP_001191196.1:p.Arg4=
XM_011513677.1:c.1A>G	XP_011511979.1:p.Met1Val
NM_000809.4:c.1A>G MANE Select	NP_000800.2:p.Met1Val
NM_001204266.2:c.12A>G	NP_001191195.1:p.Arg4=
NM_001204267.2:c.12A>G	NP_001191196.1:p.Arg4=