Canonical Allele Identifier: CA447609485
Gene: GABRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.161317965T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161890959T>A , CM000667.2:g.161890959T>A GRCh38
NC_000005.9:g.161317965T>A , CM000667.1:g.161317965T>A GRCh37
NC_000005.8:g.161250543T>A NCBI36
NG_011548.1:g.48769T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000393943.10:c.765T>A MANE Select ENSP00000377517.4:p.Ile255=
ENST00000635880.1:c.765T>A ENSP00000489738.1:p.Ile255=
ENST00000635916.2:n.2366T>A
ENST00000636340.1:c.*614T>A ENSP00000490002.1:n.*614T>A
ENST00000636408.1:n.569T>A
ENST00000636573.1:c.765T>A ENSP00000490320.1:p.Ile255=
ENST00000637044.1:c.*539T>A ENSP00000490684.1:n.*539T>A
ENST00000637827.1:c.765T>A ENSP00000490804.1:p.Ile255=
ENST00000638112.1:c.765T>A ENSP00000489839.1:p.Ile255=
ENST00000638159.1:c.810T>A ENSP00000490360.1:p.Ile270=
ENST00000023897.10:c.765T>A ENSP00000023897.6:p.Ile255=
ENST00000393943.9:c.765T>A ENSP00000377517.4:p.Ile255=
ENST00000428797.7:c.765T>A ENSP00000393097.2:p.Ile255=
ENST00000437025.6:c.765T>A ENSP00000415441.2:p.Ile255=
ENST00000519542.1:n.529T>A
ENST00000634335.1:c.765T>A ENSP00000489434.1:p.Ile255=
NM_000806.5:c.765T>A NP_000797.2:p.Ile255=
NM_001127643.1:c.765T>A NP_001121115.1:p.Ile255=
NM_001127644.1:c.765T>A NP_001121116.1:p.Ile255=
NM_001127645.1:c.765T>A NP_001121117.1:p.Ile255=
NM_001127648.1:c.765T>A NP_001121120.1:p.Ile255=
NM_001127644.2:c.765T>A MANE Select NP_001121116.1:p.Ile255=
NM_001127643.2:c.765T>A NP_001121115.1:p.Ile255=
NM_001127645.2:c.765T>A NP_001121117.1:p.Ile255=
NM_001127648.2:c.765T>A NP_001121120.1:p.Ile255=