Canonical Allele Identifier: CA1596259242
Gene: GABRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161897914T= , CM000667.2:g.161897914T= GRCh38
NC_000005.9:g.161324920T= , CM000667.1:g.161324920T= GRCh37
NC_000005.8:g.161257498T= NCBI36
NG_011548.1:g.55724T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393943.10:c.*492T= MANE Select ENSP00000377517.4:n.*492T=
ENST00000635916.2:n.4706T=
ENST00000636340.1:c.*1712T= ENSP00000490002.1:n.*1712T=
ENST00000636408.1:n.1667T=
ENST00000636573.1:c.*492T= ENSP00000490320.1:n.*492T=
ENST00000637044.1:c.*1637T= ENSP00000490684.1:n.*1637T=
ENST00000638112.1:c.*492T= ENSP00000489839.1:n.*492T=
ENST00000638159.1:c.*492T= ENSP00000490360.1:n.*492T=
ENST00000393943.9:c.*492T= ENSP00000377517.4:n.*492T=
ENST00000428797.7:c.*492T= ENSP00000393097.2:n.*492T=
ENST00000437025.6:c.*492T= ENSP00000415441.2:n.*492T=
NM_000806.5:c.*492T= NP_000797.2:n.*492T=
NM_001127643.1:c.*492T= NP_001121115.1:n.*492T=
NM_001127644.1:c.*492T= NP_001121116.1:n.*492T=
NM_001127645.1:c.*492T= NP_001121117.1:n.*492T=
NM_001127648.1:c.*492T= NP_001121120.1:n.*492T=
NM_001127644.2:c.*492T= MANE Select NP_001121116.1:n.*492T=
NM_001127643.2:c.*492T= NP_001121115.1:n.*492T=
NM_001127645.2:c.*492T= NP_001121117.1:n.*492T=
NM_001127648.2:c.*492T= NP_001121120.1:n.*492T=