Canonical Allele Identifier: CA1455119166
Gene: GABRA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46993327C= , CM000666.2:g.46993327C= GRCh38
NC_000004.11:g.46995344C= , CM000666.1:g.46995344C= GRCh37
NC_000004.10:g.46690101C= NCBI36
NG_011809.1:g.5237G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264318.4:c.86+12G= MANE Select ENSP00000264318.3:n.86+12G=
ENST00000264318.3:c.86+12G= ENSP00000264318.3:n.86+12G=
ENST00000502874.1:c.86+12G= ENSP00000424386.1:n.86+12G=
ENST00000508560.5:c.18+80G= ENSP00000425445.1:n.18+80G=
ENST00000509316.1:n.210+12G=
ENST00000511523.5:c.18+80G= ENSP00000422152.1:n.18+80G=
NM_000809.3:c.86+12G= NP_000800.2:n.86+12G=
NM_001204266.1:c.29+80G= NP_001191195.1:n.29+80G=
NM_001204267.1:c.29+80G= NP_001191196.1:n.29+80G=
XM_011513677.1:c.86+12G= XP_011511979.1:n.86+12G=
NM_000809.4:c.86+12G= MANE Select NP_000800.2:n.86+12G=
NM_001204266.2:c.29+80G= NP_001191195.1:n.29+80G=
NM_001204267.2:c.29+80G= NP_001191196.1:n.29+80G=