Canonical Allele Identifier: CA1455108213
Gene: GABRA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46971485A= , CM000666.2:g.46971485A= GRCh38
NC_000004.11:g.46973502A= , CM000666.1:g.46973502A= GRCh37
NC_000004.10:g.46668259A= NCBI36
NG_011809.1:g.27079T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264318.4:c.722-250T= MANE Select ENSP00000264318.3:n.722-250T=
ENST00000264318.3:c.722-250T= ENSP00000264318.3:n.722-250T=
ENST00000502874.1:c.*492-250T= ENSP00000424386.1:n.*492-250T=
ENST00000508560.5:c.*543-250T= ENSP00000425445.1:n.*543-250T=
ENST00000511523.5:c.*542+2747T= ENSP00000422152.1:n.*542+2747T=
NM_000809.3:c.722-250T= NP_000800.2:n.722-250T=
NM_001204266.1:c.665-250T= NP_001191195.1:n.665-250T=
NM_001204267.1:c.664+2747T= NP_001191196.1:n.664+2747T=
XM_011513677.1:c.721+2747T= XP_011511979.1:n.721+2747T=
NM_000809.4:c.722-250T= MANE Select NP_000800.2:n.722-250T=
NM_001204266.2:c.665-250T= NP_001191195.1:n.665-250T=
NM_001204267.2:c.664+2747T= NP_001191196.1:n.664+2747T=