Canonical Allele Identifier: CA2035024202
Gene: TUBA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49186694G= , CM000674.2:g.49186694G= GRCh38
NC_000012.11:g.49580477G= , CM000674.1:g.49580477G= GRCh37
NC_000012.10:g.47866744G= NCBI36
NG_008966.1:g.7385C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301071.12:c.143C= MANE Select ENSP00000301071.7:p.Ser48=
ENST00000547939.6:c.38C= ENSP00000450268.2:p.Ser13=
ENST00000550767.6:c.38C= ENSP00000446637.1:p.Ser13=
ENST00000550811.2:n.1176C=
ENST00000552924.2:c.38C= ENSP00000448725.2:p.Ser13=
ENST00000679733.1:c.143C= ENSP00000505459.1:p.Ser48=
ENST00000295766.9:c.143C= ENSP00000439020.2:p.Ser48=
ENST00000301071.11:c.143C= ENSP00000301071.7:p.Ser48=
ENST00000546918.1:c.143C= ENSP00000446613.1:p.Ser48=
ENST00000547939.5:c.38C= ENSP00000450268.1:p.Ser13=
ENST00000548363.1:n.147C=
ENST00000550254.1:n.165C=
ENST00000550767.5:c.38C= ENSP00000446637.1:p.Ser13=
ENST00000550811.1:c.38C= ENSP00000449016.1:p.Ser13=
ENST00000552924.1:c.38C= ENSP00000448725.1:p.Ser13=
NM_001270399.1:c.143C= NP_001257328.1:p.Ser48=
NM_001270400.1:c.38C= NP_001257329.1:p.Ser13=
NM_006009.3:c.143C= NP_006000.2:p.Ser48=
NM_006009.4:c.143C= MANE Select NP_006000.2:p.Ser48=
NM_001270399.2:c.143C= NP_001257328.1:p.Ser48=
NM_001270400.2:c.38C= NP_001257329.1:p.Ser13=