Canonical Allele Identifier: CA1455108198
Gene: GABRA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46971443G= , CM000666.2:g.46971443G= GRCh38
NC_000004.11:g.46973460G= , CM000666.1:g.46973460G= GRCh37
NC_000004.10:g.46668217G= NCBI36
NG_011809.1:g.27121C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264318.4:c.722-208C= MANE Select ENSP00000264318.3:n.722-208C=
ENST00000264318.3:c.722-208C= ENSP00000264318.3:n.722-208C=
ENST00000502874.1:c.*492-208C= ENSP00000424386.1:n.*492-208C=
ENST00000508560.5:c.*543-208C= ENSP00000425445.1:n.*543-208C=
ENST00000511523.5:c.*542+2789C= ENSP00000422152.1:n.*542+2789C=
NM_000809.3:c.722-208C= NP_000800.2:n.722-208C=
NM_001204266.1:c.665-208C= NP_001191195.1:n.665-208C=
NM_001204267.1:c.664+2789C= NP_001191196.1:n.664+2789C=
XM_011513677.1:c.721+2789C= XP_011511979.1:n.721+2789C=
NM_000809.4:c.722-208C= MANE Select NP_000800.2:n.722-208C=
NM_001204266.2:c.665-208C= NP_001191195.1:n.665-208C=
NM_001204267.2:c.664+2789C= NP_001191196.1:n.664+2789C=