Canonical Allele Identifier: CA1596243670

Gene: GABRA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161882664A= , CM000667.2:g.161882664A=	GRCh38
NC_000005.9:g.161309670A= , CM000667.1:g.161309670A=	GRCh37
NC_000005.8:g.161242248A=	NCBI36
NG_011548.1:g.40474A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393943.10:c.666A= MANE Select	ENSP00000377517.4:p.Gly222=
ENST00000635880.1:c.666A=	ENSP00000489738.1:p.Gly222=
ENST00000635916.2:n.2267A=
ENST00000636340.1:c.*515A=	ENSP00000490002.1:n.*515A=
ENST00000636408.1:n.470A=
ENST00000636573.1:c.666A=	ENSP00000490320.1:p.Gly222=
ENST00000637044.1:c.*440A=	ENSP00000490684.1:n.*440A=
ENST00000637827.1:c.666A=	ENSP00000490804.1:p.Gly222=
ENST00000638112.1:c.666A=	ENSP00000489839.1:p.Gly222=
ENST00000638159.1:c.711A=	ENSP00000490360.1:p.Gly237=
ENST00000023897.10:c.666A=	ENSP00000023897.6:p.Gly222=
ENST00000393943.9:c.666A=	ENSP00000377517.4:p.Gly222=
ENST00000428797.7:c.666A=	ENSP00000393097.2:p.Gly222=
ENST00000437025.6:c.666A=	ENSP00000415441.2:p.Gly222=
ENST00000519542.1:n.430A=
ENST00000634335.1:c.666A=	ENSP00000489434.1:p.Gly222=
NM_000806.5:c.666A=	NP_000797.2:p.Gly222=
NM_001127643.1:c.666A=	NP_001121115.1:p.Gly222=
NM_001127644.1:c.666A=	NP_001121116.1:p.Gly222=
NM_001127645.1:c.666A=	NP_001121117.1:p.Gly222=
NM_001127648.1:c.666A=	NP_001121120.1:p.Gly222=
NM_001127644.2:c.666A= MANE Select	NP_001121116.1:p.Gly222=
NM_001127643.2:c.666A=	NP_001121115.1:p.Gly222=
NM_001127645.2:c.666A=	NP_001121117.1:p.Gly222=
NM_001127648.2:c.666A=	NP_001121120.1:p.Gly222=