Canonical Allele Identifier: CA917182554

Gene: GABRA4

Linked Data

• dbSNP Id: rs1560488023

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993396_46993401del , CM000666.2:g.46993396_46993401del	GRCh38
NC_000004.11:g.46995413_46995418del , CM000666.1:g.46995413_46995418del	GRCh37
NC_000004.10:g.46690170_46690175del	NCBI36
NG_011809.1:g.5166_5171del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.27_32del MANE Select	ENSP00000264318.3:p.Ile10_Ala11del
ENST00000264318.3:c.27_32del	ENSP00000264318.3:p.Ile10_Ala11del
ENST00000502874.1:c.27_32del	ENSP00000424386.1:p.Ile10_Ala11del
ENST00000508560.5:c.18+9_18+14del	ENSP00000425445.1:n.18+9_18+14del
ENST00000509316.1:n.151_156del
ENST00000511523.5:c.18+9_18+14del	ENSP00000422152.1:n.18+9_18+14del
NM_000809.3:c.27_32del	NP_000800.2:p.Ile10_Ala11del
NM_001204266.1:c.29+9_29+14del	NP_001191195.1:n.29+9_29+14del
NM_001204267.1:c.29+9_29+14del	NP_001191196.1:n.29+9_29+14del
XM_011513677.1:c.27_32del	XP_011511979.1:p.Ile10_Ala11del
NM_000809.4:c.27_32del MANE Select	NP_000800.2:p.Ile10_Ala11del
NM_001204266.2:c.29+9_29+14del	NP_001191195.1:n.29+9_29+14del
NM_001204267.2:c.29+9_29+14del	NP_001191196.1:n.29+9_29+14del