Canonical Allele Identifier: CA2035022307
Gene: TUBA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49185372T= , CM000674.2:g.49185372T= GRCh38
NC_000012.11:g.49579155T= , CM000674.1:g.49579155T= GRCh37
NC_000012.10:g.47865422T= NCBI36
NG_008966.1:g.8707A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301071.12:c.994A= MANE Select ENSP00000301071.7:p.Ile332=
ENST00000547939.6:c.889A= ENSP00000450268.2:p.Ile297=
ENST00000550767.6:c.889A= ENSP00000446637.1:p.Ile297=
ENST00000550811.2:n.2027A=
ENST00000552924.2:c.889A= ENSP00000448725.2:p.Ile297=
ENST00000679733.1:c.*450A= ENSP00000505459.1:n.*450A=
ENST00000295766.9:c.994A= ENSP00000439020.2:p.Ile332=
ENST00000301071.11:c.994A= ENSP00000301071.7:p.Ile332=
ENST00000550767.5:c.889A= ENSP00000446637.1:p.Ile297=
NM_001270399.1:c.994A= NP_001257328.1:p.Ile332=
NM_001270400.1:c.889A= NP_001257329.1:p.Ile297=
NM_006009.3:c.994A= NP_006000.2:p.Ile332=
NM_006009.4:c.994A= MANE Select NP_006000.2:p.Ile332=
NM_001270399.2:c.994A= NP_001257328.1:p.Ile332=
NM_001270400.2:c.889A= NP_001257329.1:p.Ile297=