Canonical Allele Identifier: CA1455098389
Community Standard Title: NM_000809.4(GABRA4):c.1134+13106C=
Gene: GABRA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46951864G= , CM000666.2:g.46951864G= GRCh38
NC_000004.11:g.46953881G= , CM000666.1:g.46953881G= GRCh37
NC_000004.10:g.46648638G= NCBI36
NG_011809.1:g.46700C=

Transcript Alleles

HGVS Amino-acid Change
NM_000809.4:c.1134+13106C= MANE Select NP_000800.2:n.1134+13106C=
ENST00000264318.4:c.1134+13106C= MANE Select ENSP00000264318.3:n.1134+13106C=
NM_000809.3:c.1134+13106C= NP_000800.2:n.1134+13106C=
NM_001204266.1:c.1077+13106C= NP_001191195.1:n.1077+13106C=
NM_001204266.2:c.1077+13106C= NP_001191195.1:n.1077+13106C=
NM_001204267.1:c.924+13106C= NP_001191196.1:n.924+13106C=
NM_001204267.2:c.924+13106C= NP_001191196.1:n.924+13106C=
ENST00000264318.3:c.1134+13106C= ENSP00000264318.3:n.1134+13106C=
ENST00000508560.5:c.*955+13106C= ENSP00000425445.1:n.*955+13106C=
ENST00000511523.5:c.*802+13106C= ENSP00000422152.1:n.*802+13106C=
XM_011513677.1:c.981+13106C= XP_011511979.1:n.981+13106C=