Canonical Allele Identifier: CA362178964

Gene: GABRA1

Linked Data

• dbSNP Id: rs1265026103
• gnomAD v2: 5-161300253-A-G
• gnomAD v4: 5-161873247-A-G
• MyVariant Identifiers: chr5:g.161300253A>G (hg19) ; chr5:g.161873247A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161873247A>G , CM000667.2:g.161873247A>G	GRCh38
NC_000005.9:g.161300253A>G , CM000667.1:g.161300253A>G	GRCh37
NC_000005.8:g.161232831A>G	NCBI36
NG_011548.1:g.31057A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393943.10:c.386A>G MANE Select	ENSP00000377517.4:p.His129Arg
ENST00000635880.1:c.386A>G	ENSP00000489738.1:p.His129Arg
ENST00000635916.2:n.1161A>G
ENST00000636340.1:c.*235A>G	ENSP00000490002.1:n.*235A>G
ENST00000636408.1:n.190A>G
ENST00000636573.1:c.386A>G	ENSP00000490320.1:p.His129Arg
ENST00000637044.1:c.*160A>G	ENSP00000490684.1:n.*160A>G
ENST00000637827.1:c.386A>G	ENSP00000490804.1:p.His129Arg
ENST00000638112.1:c.386A>G	ENSP00000489839.1:p.His129Arg
ENST00000638159.1:c.431A>G	ENSP00000490360.1:p.His144Arg
ENST00000023897.10:c.386A>G	ENSP00000023897.6:p.His129Arg
ENST00000393943.9:c.386A>G	ENSP00000377517.4:p.His129Arg
ENST00000428797.7:c.386A>G	ENSP00000393097.2:p.His129Arg
ENST00000437025.6:c.386A>G	ENSP00000415441.2:p.His129Arg
ENST00000519542.1:n.150A>G
ENST00000519621.2:c.386A>G	ENSP00000430435.2:p.His129Arg
ENST00000634335.1:c.386A>G	ENSP00000489434.1:p.His129Arg
NM_000806.5:c.386A>G	NP_000797.2:p.His129Arg
NM_001127643.1:c.386A>G	NP_001121115.1:p.His129Arg
NM_001127644.1:c.386A>G	NP_001121116.1:p.His129Arg
NM_001127645.1:c.386A>G	NP_001121117.1:p.His129Arg
NM_001127648.1:c.386A>G	NP_001121120.1:p.His129Arg
NM_001127644.2:c.386A>G MANE Select	NP_001121116.1:p.His129Arg
NM_001127643.2:c.386A>G	NP_001121115.1:p.His129Arg
NM_001127645.2:c.386A>G	NP_001121117.1:p.His129Arg
NM_001127648.2:c.386A>G	NP_001121120.1:p.His129Arg