Canonical Allele Identifier: CA2035022206
Gene: TUBA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49185290G= , CM000674.2:g.49185290G= GRCh38
NC_000012.11:g.49579073G= , CM000674.1:g.49579073G= GRCh37
NC_000012.10:g.47865340G= NCBI36
NG_008966.1:g.8789C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301071.12:c.1076C= MANE Select ENSP00000301071.7:p.Pro359=
ENST00000547939.6:c.971C= ENSP00000450268.2:p.Pro324=
ENST00000550767.6:c.971C= ENSP00000446637.1:p.Pro324=
ENST00000550811.2:n.2109C=
ENST00000552924.2:c.971C= ENSP00000448725.2:p.Pro324=
ENST00000679733.1:c.*532C= ENSP00000505459.1:n.*532C=
ENST00000295766.9:c.1076C= ENSP00000439020.2:p.Pro359=
ENST00000301071.11:c.1076C= ENSP00000301071.7:p.Pro359=
ENST00000550767.5:c.971C= ENSP00000446637.1:p.Pro324=
NM_001270399.1:c.1076C= NP_001257328.1:p.Pro359=
NM_001270400.1:c.971C= NP_001257329.1:p.Pro324=
NM_006009.3:c.1076C= NP_006000.2:p.Pro359=
NM_006009.4:c.1076C= MANE Select NP_006000.2:p.Pro359=
NM_001270399.2:c.1076C= NP_001257328.1:p.Pro359=
NM_001270400.2:c.971C= NP_001257329.1:p.Pro324=