Canonical Allele Identifier: CA1596234653

Gene: GABRA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161873440_161873441delinsCT , CM000667.2:g.161873440_161873441delinsCT	GRCh38
NC_000005.9:g.161300446_161300447delinsCT , CM000667.1:g.161300446_161300447delinsCT	GRCh37
NC_000005.8:g.161233024_161233025delinsCT	NCBI36
NG_011548.1:g.31250_31251delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393943.10:c.476+103_476+104delinsCT MANE Select	ENSP00000377517.4:n.476+103_476+104delinsCT
ENST00000635880.1:c.476+103_476+104delinsCT	ENSP00000489738.1:n.476+103_476+104delinsCT
ENST00000635916.2:n.1251+103_1251+104delinsCT
ENST00000636340.1:c.*325+103_*325+104delinsCT	ENSP00000490002.1:n.*325+103_*325+104delinsCT
ENST00000636408.1:n.280+103_280+104delinsCT
ENST00000636573.1:c.476+103_476+104delinsCT	ENSP00000490320.1:n.476+103_476+104delinsCT
ENST00000637044.1:c.*250+103_*250+104delinsCT	ENSP00000490684.1:n.*250+103_*250+104delinsCT
ENST00000637827.1:c.476+103_476+104delinsCT	ENSP00000490804.1:n.476+103_476+104delinsCT
ENST00000638112.1:c.476+103_476+104delinsCT	ENSP00000489839.1:n.476+103_476+104delinsCT
ENST00000638159.1:c.521+103_521+104delinsCT	ENSP00000490360.1:n.521+103_521+104delinsCT
ENST00000023897.10:c.476+103_476+104delinsCT	ENSP00000023897.6:n.476+103_476+104delinsCT
ENST00000393943.9:c.476+103_476+104delinsCT	ENSP00000377517.4:n.476+103_476+104delinsCT
ENST00000428797.7:c.476+103_476+104delinsCT	ENSP00000393097.2:n.476+103_476+104delinsCT
ENST00000437025.6:c.476+103_476+104delinsCT	ENSP00000415441.2:n.476+103_476+104delinsCT
ENST00000519542.1:n.240+103_240+104delinsCT
ENST00000519621.2:c.476+103_476+104delinsCT	ENSP00000430435.2:n.476+103_476+104delinsCT
ENST00000634335.1:c.476+103_476+104delinsCT	ENSP00000489434.1:n.476+103_476+104delinsCT
NM_000806.5:c.476+103_476+104delinsCT	NP_000797.2:n.476+103_476+104delinsCT
NM_001127643.1:c.476+103_476+104delinsCT	NP_001121115.1:n.476+103_476+104delinsCT
NM_001127644.1:c.476+103_476+104delinsCT	NP_001121116.1:n.476+103_476+104delinsCT
NM_001127645.1:c.476+103_476+104delinsCT	NP_001121117.1:n.476+103_476+104delinsCT
NM_001127648.1:c.476+103_476+104delinsCT	NP_001121120.1:n.476+103_476+104delinsCT
NM_001127644.2:c.476+103_476+104delinsCT MANE Select	NP_001121116.1:n.476+103_476+104delinsCT
NM_001127643.2:c.476+103_476+104delinsCT	NP_001121115.1:n.476+103_476+104delinsCT
NM_001127645.2:c.476+103_476+104delinsCT	NP_001121117.1:n.476+103_476+104delinsCT
NM_001127648.2:c.476+103_476+104delinsCT	NP_001121120.1:n.476+103_476+104delinsCT