Canonical Allele Identifier: CA1455119075

Gene: GABRA4

Linked Data

• dbSNP Id: rs1723838701

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993174T>G , CM000666.2:g.46993174T>G	GRCh38
NC_000004.11:g.46995191T>G , CM000666.1:g.46995191T>G	GRCh37
NC_000004.10:g.46689948T>G	NCBI36
NG_011809.1:g.5390A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.86+165A>C MANE Select	ENSP00000264318.3:n.86+165A>C
ENST00000264318.3:c.86+165A>C	ENSP00000264318.3:n.86+165A>C
ENST00000502874.1:c.86+165A>C	ENSP00000424386.1:n.86+165A>C
ENST00000508560.5:c.19-228A>C	ENSP00000425445.1:n.19-228A>C
ENST00000509316.1:n.210+165A>C
ENST00000511523.5:c.19-228A>C	ENSP00000422152.1:n.19-228A>C
NM_000809.3:c.86+165A>C	NP_000800.2:n.86+165A>C
NM_001204266.1:c.30-228A>C	NP_001191195.1:n.30-228A>C
NM_001204267.1:c.30-228A>C	NP_001191196.1:n.30-228A>C
XM_011513677.1:c.86+165A>C	XP_011511979.1:n.86+165A>C
NM_000809.4:c.86+165A>C MANE Select	NP_000800.2:n.86+165A>C
NM_001204266.2:c.30-228A>C	NP_001191195.1:n.30-228A>C
NM_001204267.2:c.30-228A>C	NP_001191196.1:n.30-228A>C