Canonical Allele Identifier: CA1455086552
Gene: GABRA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46927483A= , CM000666.2:g.46927483A= GRCh38
NC_000004.11:g.46929500A= , CM000666.1:g.46929500A= GRCh37
NC_000004.10:g.46624257A= NCBI36
NG_011809.1:g.71081T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264318.4:c.*742T= MANE Select ENSP00000264318.3:n.*742T=
ENST00000264318.3:c.*742T= ENSP00000264318.3:n.*742T=
NM_000809.3:c.*742T= NP_000800.2:n.*742T=
NM_001204266.1:c.*742T= NP_001191195.1:n.*742T=
NM_001204267.1:c.*742T= NP_001191196.1:n.*742T=
XM_011513677.1:c.*742T= XP_011511979.1:n.*742T=
NM_000809.4:c.*742T= MANE Select NP_000800.2:n.*742T=
NM_001204266.2:c.*742T= NP_001191195.1:n.*742T=
NM_001204267.2:c.*742T= NP_001191196.1:n.*742T=