Canonical Allele Identifier: CA2035023055
Gene: TUBA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49185823T= , CM000674.2:g.49185823T= GRCh38
NC_000012.11:g.49579606T= , CM000674.1:g.49579606T= GRCh37
NC_000012.10:g.47865873T= NCBI36
NG_008966.1:g.8256A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301071.12:c.543A= MANE Select ENSP00000301071.7:p.Val181=
ENST00000547939.6:c.438A= ENSP00000450268.2:p.Val146=
ENST00000550767.6:c.438A= ENSP00000446637.1:p.Val146=
ENST00000550811.2:n.1576A=
ENST00000552924.2:c.438A= ENSP00000448725.2:p.Val146=
ENST00000679733.1:c.566A= ENSP00000505459.1:p.Ter189=
ENST00000295766.9:c.543A= ENSP00000439020.2:p.Val181=
ENST00000301071.11:c.543A= ENSP00000301071.7:p.Val181=
ENST00000546918.1:c.695A= ENSP00000446613.1:p.Ter232=
ENST00000547939.5:c.438A= ENSP00000450268.1:p.Val146=
ENST00000550767.5:c.438A= ENSP00000446637.1:p.Val146=
NM_001270399.1:c.543A= NP_001257328.1:p.Val181=
NM_001270400.1:c.438A= NP_001257329.1:p.Val146=
NM_006009.3:c.543A= NP_006000.2:p.Val181=
NM_006009.4:c.543A= MANE Select NP_006000.2:p.Val181=
NM_001270399.2:c.543A= NP_001257328.1:p.Val181=
NM_001270400.2:c.438A= NP_001257329.1:p.Val146=