Canonical Allele Identifier: CA1455107465
Gene: GABRA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46969992A= , CM000666.2:g.46969992A= GRCh38
NC_000004.11:g.46972009A= , CM000666.1:g.46972009A= GRCh37
NC_000004.10:g.46666766A= NCBI36
NG_011809.1:g.28572T=

Transcript Alleles

HGVS Amino-acid Change
NM_000809.4:c.874+1091T= MANE Select NP_000800.2:n.874+1091T=
ENST00000264318.4:c.874+1091T= MANE Select ENSP00000264318.3:n.874+1091T=
NM_000809.3:c.874+1091T= NP_000800.2:n.874+1091T=
NM_001204266.1:c.817+1091T= NP_001191195.1:n.817+1091T=
NM_001204266.2:c.817+1091T= NP_001191195.1:n.817+1091T=
NM_001204267.1:c.664+4240T= NP_001191196.1:n.664+4240T=
NM_001204267.2:c.664+4240T= NP_001191196.1:n.664+4240T=
ENST00000264318.3:c.874+1091T= ENSP00000264318.3:n.874+1091T=
ENST00000508560.5:c.*695+1091T= ENSP00000425445.1:n.*695+1091T=
ENST00000511523.5:c.*542+4240T= ENSP00000422152.1:n.*542+4240T=
XM_011513677.1:c.721+4240T= XP_011511979.1:n.721+4240T=