Canonical Allele Identifier: CA1455108161

Gene: GABRA4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46971345_46971346delinsCT , CM000666.2:g.46971345_46971346delinsCT	GRCh38
NC_000004.11:g.46973362_46973363delinsCT , CM000666.1:g.46973362_46973363delinsCT	GRCh37
NC_000004.10:g.46668119_46668120delinsCT	NCBI36
NG_011809.1:g.27218_27219delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.722-111_722-110delinsAG MANE Select	ENSP00000264318.3:n.722-111_722-110delinsAG
ENST00000264318.3:c.722-111_722-110delinsAG	ENSP00000264318.3:n.722-111_722-110delinsAG
ENST00000502874.1:c.*492-111_*492-110delinsAG	ENSP00000424386.1:n.*492-111_*492-110delinsAG
ENST00000508560.5:c.*543-111_*543-110delinsAG	ENSP00000425445.1:n.*543-111_*543-110delinsAG
ENST00000511523.5:c.*542+2886_*542+2887delinsAG	ENSP00000422152.1:n.*542+2886_*542+2887delinsAG
NM_000809.3:c.722-111_722-110delinsAG	NP_000800.2:n.722-111_722-110delinsAG
NM_001204266.1:c.665-111_665-110delinsAG	NP_001191195.1:n.665-111_665-110delinsAG
NM_001204267.1:c.664+2886_664+2887delinsAG	NP_001191196.1:n.664+2886_664+2887delinsAG
XM_011513677.1:c.721+2886_721+2887delinsAG	XP_011511979.1:n.721+2886_721+2887delinsAG
NM_000809.4:c.722-111_722-110delinsAG MANE Select	NP_000800.2:n.722-111_722-110delinsAG
NM_001204266.2:c.665-111_665-110delinsAG	NP_001191195.1:n.665-111_665-110delinsAG
NM_001204267.2:c.664+2886_664+2887delinsAG	NP_001191196.1:n.664+2886_664+2887delinsAG