Canonical Allele Identifier: CA1455119221
Gene: GABRA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46993483A= , CM000666.2:g.46993483A= GRCh38
NC_000004.11:g.46995500A= , CM000666.1:g.46995500A= GRCh37
NC_000004.10:g.46690257A= NCBI36
NG_011809.1:g.5081T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264318.4:c.-59T= MANE Select ENSP00000264318.3:n.-59T=
ENST00000264318.3:c.-59T= ENSP00000264318.3:n.-59T=
ENST00000502874.1:c.-59T= ENSP00000424386.1:n.-59T=
ENST00000508560.5:c.-59T= ENSP00000425445.1:n.-59T=
ENST00000509316.1:n.66T=
ENST00000511523.5:c.-59T= ENSP00000422152.1:n.-59T=
NM_000809.3:c.-59T= NP_000800.2:n.-59T=
NM_001204266.1:c.-48T= NP_001191195.1:n.-48T=
NM_001204267.1:c.-48T= NP_001191196.1:n.-48T=
XM_011513677.1:c.-59T= XP_011511979.1:n.-59T=
NM_000809.4:c.-59T= MANE Select NP_000800.2:n.-59T=
NM_001204266.2:c.-48T= NP_001191195.1:n.-48T=
NM_001204267.2:c.-48T= NP_001191196.1:n.-48T=