Canonical Allele Identifier: CA1455086598
Gene: GABRA4 HGNC NCBI

Linked Data

dbSNP Id: rs1721272026

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46927618T>C , CM000666.2:g.46927618T>C GRCh38
NC_000004.11:g.46929635T>C , CM000666.1:g.46929635T>C GRCh37
NC_000004.10:g.46624392T>C NCBI36
NG_011809.1:g.70946A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264318.4:c.*607A>G MANE Select ENSP00000264318.3:n.*607A>G
ENST00000264318.3:c.*607A>G ENSP00000264318.3:n.*607A>G
NM_000809.3:c.*607A>G NP_000800.2:n.*607A>G
NM_001204266.1:c.*607A>G NP_001191195.1:n.*607A>G
NM_001204267.1:c.*607A>G NP_001191196.1:n.*607A>G
XM_011513677.1:c.*607A>G XP_011511979.1:n.*607A>G
NM_000809.4:c.*607A>G MANE Select NP_000800.2:n.*607A>G
NM_001204266.2:c.*607A>G NP_001191195.1:n.*607A>G
NM_001204267.2:c.*607A>G NP_001191196.1:n.*607A>G