Canonical Allele Identifier: CA2035022695
Gene: TUBA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49185499T= , CM000674.2:g.49185499T= GRCh38
NC_000012.11:g.49579282T= , CM000674.1:g.49579282T= GRCh37
NC_000012.10:g.47865549T= NCBI36
NG_008966.1:g.8580A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301071.12:c.867A= MANE Select ENSP00000301071.7:p.Ala289=
ENST00000547939.6:c.762A= ENSP00000450268.2:p.Ala254=
ENST00000550767.6:c.762A= ENSP00000446637.1:p.Ala254=
ENST00000550811.2:n.1900A=
ENST00000552924.2:c.762A= ENSP00000448725.2:p.Ala254=
ENST00000679733.1:c.*323A= ENSP00000505459.1:n.*323A=
ENST00000295766.9:c.867A= ENSP00000439020.2:p.Ala289=
ENST00000301071.11:c.867A= ENSP00000301071.7:p.Ala289=
ENST00000550767.5:c.762A= ENSP00000446637.1:p.Ala254=
NM_001270399.1:c.867A= NP_001257328.1:p.Ala289=
NM_001270400.1:c.762A= NP_001257329.1:p.Ala254=
NM_006009.3:c.867A= NP_006000.2:p.Ala289=
NM_006009.4:c.867A= MANE Select NP_006000.2:p.Ala289=
NM_001270399.2:c.867A= NP_001257328.1:p.Ala289=
NM_001270400.2:c.762A= NP_001257329.1:p.Ala254=