Canonical Allele Identifier: CA3544342
Gene: GABRA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 536749
dbSNP Id: rs769743354

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161854177C>A , CM000667.2:g.161854177C>A GRCh38
NC_000005.9:g.161281183C>A , CM000667.1:g.161281183C>A GRCh37
NC_000005.8:g.161213761C>A NCBI36
NG_011548.1:g.11987C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000393943.10:c.94C>A MANE Select ENSP00000377517.4:p.Gln32Lys
ENST00000635880.1:c.94C>A ENSP00000489738.1:p.Gln32Lys
ENST00000635916.2:n.869C>A
ENST00000636340.1:c.156C>A ENSP00000490002.1:p.Tyr52Ter
ENST00000636573.1:c.94C>A ENSP00000490320.1:p.Gln32Lys
ENST00000637044.1:c.94C>A ENSP00000490684.1:p.Gln32Lys
ENST00000637827.1:c.94C>A ENSP00000490804.1:p.Gln32Lys
ENST00000638112.1:c.94C>A ENSP00000489839.1:p.Gln32Lys
ENST00000638159.1:c.139C>A ENSP00000490360.1:p.Gln47Lys
ENST00000023897.10:c.94C>A ENSP00000023897.6:p.Gln32Lys
ENST00000393943.9:c.94C>A ENSP00000377517.4:p.Gln32Lys
ENST00000428797.7:c.94C>A ENSP00000393097.2:p.Gln32Lys
ENST00000437025.6:c.94C>A ENSP00000415441.2:p.Gln32Lys
ENST00000519621.2:c.94C>A ENSP00000430435.2:p.Gln32Lys
ENST00000521339.5:c.112C>A ENSP00000430895.1:p.Gln38Lys
ENST00000522651.6:c.157C>A ENSP00000430507.2:p.Gln53Lys
ENST00000634335.1:c.94C>A ENSP00000489434.1:p.Gln32Lys
ENST00000635096.1:c.94C>A ENSP00000489033.1:p.Gln32Lys
NM_000806.5:c.94C>A NP_000797.2:p.Gln32Lys
NM_001127643.1:c.94C>A NP_001121115.1:p.Gln32Lys
NM_001127644.1:c.94C>A NP_001121116.1:p.Gln32Lys
NM_001127645.1:c.94C>A NP_001121117.1:p.Gln32Lys
NM_001127648.1:c.94C>A NP_001121120.1:p.Gln32Lys
NM_001127644.2:c.94C>A MANE Select NP_001121116.1:p.Gln32Lys
NM_001127643.2:c.94C>A NP_001121115.1:p.Gln32Lys
NM_001127645.2:c.94C>A NP_001121117.1:p.Gln32Lys
NM_001127648.2:c.94C>A NP_001121120.1:p.Gln32Lys