Canonical Allele Identifier: CA439168766

Gene: GABRA4

Linked Data

• MyVariant Identifiers: chr4:g.46995433A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993416A>G , CM000666.2:g.46993416A>G	GRCh38
NC_000004.11:g.46995433A>G , CM000666.1:g.46995433A>G	GRCh37
NC_000004.10:g.46690190A>G	NCBI36
NG_011809.1:g.5148T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.9T>C MANE Select	ENSP00000264318.3:p.Ser3=
ENST00000264318.3:c.9T>C	ENSP00000264318.3:p.Ser3=
ENST00000502874.1:c.9T>C	ENSP00000424386.1:p.Ser3=
ENST00000508560.5:c.9T>C	ENSP00000425445.1:p.Ser3=
ENST00000509316.1:n.133T>C
ENST00000511523.5:c.9T>C	ENSP00000422152.1:p.Ser3=
NM_000809.3:c.9T>C	NP_000800.2:p.Ser3=
NM_001204266.1:c.20T>C	NP_001191195.1:p.Leu7Pro
NM_001204267.1:c.20T>C	NP_001191196.1:p.Leu7Pro
XM_011513677.1:c.9T>C	XP_011511979.1:p.Ser3=
NM_000809.4:c.9T>C MANE Select	NP_000800.2:p.Ser3=
NM_001204266.2:c.20T>C	NP_001191195.1:p.Leu7Pro
NM_001204267.2:c.20T>C	NP_001191196.1:p.Leu7Pro