Canonical Allele Identifier: CA1455119208
Gene: GABRA4 HGNC NCBI

Linked Data

dbSNP Id: rs1723856804

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46993447A>G , CM000666.2:g.46993447A>G GRCh38
NC_000004.11:g.46995464A>G , CM000666.1:g.46995464A>G GRCh37
NC_000004.10:g.46690221A>G NCBI36
NG_011809.1:g.5117T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264318.4:c.-23T>C MANE Select ENSP00000264318.3:n.-23T>C
ENST00000264318.3:c.-23T>C ENSP00000264318.3:n.-23T>C
ENST00000502874.1:c.-23T>C ENSP00000424386.1:n.-23T>C
ENST00000508560.5:c.-23T>C ENSP00000425445.1:n.-23T>C
ENST00000509316.1:n.102T>C
ENST00000511523.5:c.-23T>C ENSP00000422152.1:n.-23T>C
NM_000809.3:c.-23T>C NP_000800.2:n.-23T>C
NM_001204266.1:c.-12T>C NP_001191195.1:n.-12T>C
NM_001204267.1:c.-12T>C NP_001191196.1:n.-12T>C
XM_011513677.1:c.-23T>C XP_011511979.1:n.-23T>C
NM_000809.4:c.-23T>C MANE Select NP_000800.2:n.-23T>C
NM_001204266.2:c.-12T>C NP_001191195.1:n.-12T>C
NM_001204267.2:c.-12T>C NP_001191196.1:n.-12T>C