Canonical Allele Identifier: CA1455108197
Gene: GABRA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46971442C= , CM000666.2:g.46971442C= GRCh38
NC_000004.11:g.46973459C= , CM000666.1:g.46973459C= GRCh37
NC_000004.10:g.46668216C= NCBI36
NG_011809.1:g.27122G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264318.4:c.722-207G= MANE Select ENSP00000264318.3:n.722-207G=
ENST00000264318.3:c.722-207G= ENSP00000264318.3:n.722-207G=
ENST00000502874.1:c.*492-207G= ENSP00000424386.1:n.*492-207G=
ENST00000508560.5:c.*543-207G= ENSP00000425445.1:n.*543-207G=
ENST00000511523.5:c.*542+2790G= ENSP00000422152.1:n.*542+2790G=
NM_000809.3:c.722-207G= NP_000800.2:n.722-207G=
NM_001204266.1:c.665-207G= NP_001191195.1:n.665-207G=
NM_001204267.1:c.664+2790G= NP_001191196.1:n.664+2790G=
XM_011513677.1:c.721+2790G= XP_011511979.1:n.721+2790G=
NM_000809.4:c.722-207G= MANE Select NP_000800.2:n.722-207G=
NM_001204266.2:c.665-207G= NP_001191195.1:n.665-207G=
NM_001204267.2:c.664+2790G= NP_001191196.1:n.664+2790G=