Canonical Allele Identifier: CA384633995
Gene: TUBA1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49185111A>T , CM000674.2:g.49185111A>T GRCh38
NC_000012.11:g.49578894A>T , CM000674.1:g.49578894A>T GRCh37
NC_000012.10:g.47865161A>T NCBI36
NG_008966.1:g.8968T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301071.12:c.1255T>A MANE Select ENSP00000301071.7:p.Ser419Thr
ENST00000547939.6:c.1150T>A ENSP00000450268.2:p.Ser384Thr
ENST00000550767.6:c.1150T>A ENSP00000446637.1:p.Ser384Thr
ENST00000550811.2:n.2288T>A
ENST00000552924.2:c.1150T>A ENSP00000448725.2:p.Ser384Thr
ENST00000679733.1:c.*711T>A ENSP00000505459.1:n.*711T>A
ENST00000295766.9:c.1255T>A ENSP00000439020.2:p.Ser419Thr
ENST00000301071.11:c.1255T>A ENSP00000301071.7:p.Ser419Thr
ENST00000550767.5:c.1150T>A ENSP00000446637.1:p.Ser384Thr
NM_001270399.1:c.1255T>A NP_001257328.1:p.Ser419Thr
NM_001270400.1:c.1150T>A NP_001257329.1:p.Ser384Thr
NM_006009.3:c.1255T>A NP_006000.2:p.Ser419Thr
NM_006009.4:c.1255T>A MANE Select NP_006000.2:p.Ser419Thr
NM_001270399.2:c.1255T>A NP_001257328.1:p.Ser419Thr
NM_001270400.2:c.1150T>A NP_001257329.1:p.Ser384Thr