Canonical Allele Identifier: CA1455119059

Gene: GABRA4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993151_46993152delinsTG , CM000666.2:g.46993151_46993152delinsTG	GRCh38
NC_000004.11:g.46995168_46995169delinsTG , CM000666.1:g.46995168_46995169delinsTG	GRCh37
NC_000004.10:g.46689925_46689926delinsTG	NCBI36
NG_011809.1:g.5412_5413delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.86+187_86+188delinsCA MANE Select	ENSP00000264318.3:n.86+187_86+188delinsCA
ENST00000264318.3:c.86+187_86+188delinsCA	ENSP00000264318.3:n.86+187_86+188delinsCA
ENST00000502874.1:c.86+187_86+188delinsCA	ENSP00000424386.1:n.86+187_86+188delinsCA
ENST00000508560.5:c.19-206_19-205delinsCA	ENSP00000425445.1:n.19-206_19-205delinsCA
ENST00000509316.1:n.210+187_210+188delinsCA
ENST00000511523.5:c.19-206_19-205delinsCA	ENSP00000422152.1:n.19-206_19-205delinsCA
NM_000809.3:c.86+187_86+188delinsCA	NP_000800.2:n.86+187_86+188delinsCA
NM_001204266.1:c.30-206_30-205delinsCA	NP_001191195.1:n.30-206_30-205delinsCA
NM_001204267.1:c.30-206_30-205delinsCA	NP_001191196.1:n.30-206_30-205delinsCA
XM_011513677.1:c.86+187_86+188delinsCA	XP_011511979.1:n.86+187_86+188delinsCA
NM_000809.4:c.86+187_86+188delinsCA MANE Select	NP_000800.2:n.86+187_86+188delinsCA
NM_001204266.2:c.30-206_30-205delinsCA	NP_001191195.1:n.30-206_30-205delinsCA
NM_001204267.2:c.30-206_30-205delinsCA	NP_001191196.1:n.30-206_30-205delinsCA