Canonical Allele Identifier: CA1455108192
Gene: GABRA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46971426G= , CM000666.2:g.46971426G= GRCh38
NC_000004.11:g.46973443G= , CM000666.1:g.46973443G= GRCh37
NC_000004.10:g.46668200G= NCBI36
NG_011809.1:g.27138C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264318.4:c.722-191C= MANE Select ENSP00000264318.3:n.722-191C=
ENST00000264318.3:c.722-191C= ENSP00000264318.3:n.722-191C=
ENST00000502874.1:c.*492-191C= ENSP00000424386.1:n.*492-191C=
ENST00000508560.5:c.*543-191C= ENSP00000425445.1:n.*543-191C=
ENST00000511523.5:c.*542+2806C= ENSP00000422152.1:n.*542+2806C=
NM_000809.3:c.722-191C= NP_000800.2:n.722-191C=
NM_001204266.1:c.665-191C= NP_001191195.1:n.665-191C=
NM_001204267.1:c.664+2806C= NP_001191196.1:n.664+2806C=
XM_011513677.1:c.721+2806C= XP_011511979.1:n.721+2806C=
NM_000809.4:c.722-191C= MANE Select NP_000800.2:n.722-191C=
NM_001204266.2:c.665-191C= NP_001191195.1:n.665-191C=
NM_001204267.2:c.664+2806C= NP_001191196.1:n.664+2806C=