Canonical Allele Identifier: CA1455086606
Gene: GABRA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46927635A= , CM000666.2:g.46927635A= GRCh38
NC_000004.11:g.46929652A= , CM000666.1:g.46929652A= GRCh37
NC_000004.10:g.46624409A= NCBI36
NG_011809.1:g.70929T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264318.4:c.*590T= MANE Select ENSP00000264318.3:n.*590T=
ENST00000264318.3:c.*590T= ENSP00000264318.3:n.*590T=
NM_000809.3:c.*590T= NP_000800.2:n.*590T=
NM_001204266.1:c.*590T= NP_001191195.1:n.*590T=
NM_001204267.1:c.*590T= NP_001191196.1:n.*590T=
XM_011513677.1:c.*590T= XP_011511979.1:n.*590T=
NM_000809.4:c.*590T= MANE Select NP_000800.2:n.*590T=
NM_001204266.2:c.*590T= NP_001191195.1:n.*590T=
NM_001204267.2:c.*590T= NP_001191196.1:n.*590T=