Canonical Allele Identifier: CA1455119070
Gene: GABRA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46993166T= , CM000666.2:g.46993166T= GRCh38
NC_000004.11:g.46995183T= , CM000666.1:g.46995183T= GRCh37
NC_000004.10:g.46689940T= NCBI36
NG_011809.1:g.5398A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264318.4:c.86+173A= MANE Select ENSP00000264318.3:n.86+173A=
ENST00000264318.3:c.86+173A= ENSP00000264318.3:n.86+173A=
ENST00000502874.1:c.86+173A= ENSP00000424386.1:n.86+173A=
ENST00000508560.5:c.19-220A= ENSP00000425445.1:n.19-220A=
ENST00000509316.1:n.210+173A=
ENST00000511523.5:c.19-220A= ENSP00000422152.1:n.19-220A=
NM_000809.3:c.86+173A= NP_000800.2:n.86+173A=
NM_001204266.1:c.30-220A= NP_001191195.1:n.30-220A=
NM_001204267.1:c.30-220A= NP_001191196.1:n.30-220A=
XM_011513677.1:c.86+173A= XP_011511979.1:n.86+173A=
NM_000809.4:c.86+173A= MANE Select NP_000800.2:n.86+173A=
NM_001204266.2:c.30-220A= NP_001191195.1:n.30-220A=
NM_001204267.2:c.30-220A= NP_001191196.1:n.30-220A=