Canonical Allele Identifier: CA1455119078
Gene: GABRA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46993177G= , CM000666.2:g.46993177G= GRCh38
NC_000004.11:g.46995194G= , CM000666.1:g.46995194G= GRCh37
NC_000004.10:g.46689951G= NCBI36
NG_011809.1:g.5387C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264318.4:c.86+162C= MANE Select ENSP00000264318.3:n.86+162C=
ENST00000264318.3:c.86+162C= ENSP00000264318.3:n.86+162C=
ENST00000502874.1:c.86+162C= ENSP00000424386.1:n.86+162C=
ENST00000508560.5:c.19-231C= ENSP00000425445.1:n.19-231C=
ENST00000509316.1:n.210+162C=
ENST00000511523.5:c.19-231C= ENSP00000422152.1:n.19-231C=
NM_000809.3:c.86+162C= NP_000800.2:n.86+162C=
NM_001204266.1:c.30-231C= NP_001191195.1:n.30-231C=
NM_001204267.1:c.30-231C= NP_001191196.1:n.30-231C=
XM_011513677.1:c.86+162C= XP_011511979.1:n.86+162C=
NM_000809.4:c.86+162C= MANE Select NP_000800.2:n.86+162C=
NM_001204266.2:c.30-231C= NP_001191195.1:n.30-231C=
NM_001204267.2:c.30-231C= NP_001191196.1:n.30-231C=