Canonical Allele Identifier: CA1596259182
Gene: GABRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161897814T= , CM000667.2:g.161897814T= GRCh38
NC_000005.9:g.161324820T= , CM000667.1:g.161324820T= GRCh37
NC_000005.8:g.161257398T= NCBI36
NG_011548.1:g.55624T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393943.10:c.*392T= MANE Select ENSP00000377517.4:n.*392T=
ENST00000635916.2:n.4606T=
ENST00000636340.1:c.*1612T= ENSP00000490002.1:n.*1612T=
ENST00000636408.1:n.1567T=
ENST00000636573.1:c.*392T= ENSP00000490320.1:n.*392T=
ENST00000637044.1:c.*1537T= ENSP00000490684.1:n.*1537T=
ENST00000638112.1:c.*392T= ENSP00000489839.1:n.*392T=
ENST00000638159.1:c.*392T= ENSP00000490360.1:n.*392T=
ENST00000393943.9:c.*392T= ENSP00000377517.4:n.*392T=
ENST00000428797.7:c.*392T= ENSP00000393097.2:n.*392T=
ENST00000437025.6:c.*392T= ENSP00000415441.2:n.*392T=
NM_000806.5:c.*392T= NP_000797.2:n.*392T=
NM_001127643.1:c.*392T= NP_001121115.1:n.*392T=
NM_001127644.1:c.*392T= NP_001121116.1:n.*392T=
NM_001127645.1:c.*392T= NP_001121117.1:n.*392T=
NM_001127648.1:c.*392T= NP_001121120.1:n.*392T=
NM_001127644.2:c.*392T= MANE Select NP_001121116.1:n.*392T=
NM_001127643.2:c.*392T= NP_001121115.1:n.*392T=
NM_001127645.2:c.*392T= NP_001121117.1:n.*392T=
NM_001127648.2:c.*392T= NP_001121120.1:n.*392T=