Canonical Allele Identifier: CA384640421
Gene: TUBA1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49185650G>C , CM000674.2:g.49185650G>C GRCh38
NC_000012.11:g.49579433G>C , CM000674.1:g.49579433G>C GRCh37
NC_000012.10:g.47865700G>C NCBI36
NG_008966.1:g.8429C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301071.12:c.716C>G MANE Select ENSP00000301071.7:p.Thr239Ser
ENST00000547939.6:c.611C>G ENSP00000450268.2:p.Thr204Ser
ENST00000550767.6:c.611C>G ENSP00000446637.1:p.Thr204Ser
ENST00000550811.2:n.1749C>G
ENST00000552924.2:c.611C>G ENSP00000448725.2:p.Thr204Ser
ENST00000679733.1:c.*172C>G ENSP00000505459.1:n.*172C>G
ENST00000295766.9:c.716C>G ENSP00000439020.2:p.Thr239Ser
ENST00000301071.11:c.716C>G ENSP00000301071.7:p.Thr239Ser
ENST00000546918.1:c.*172C>G ENSP00000446613.1:n.*172C>G
ENST00000547939.5:c.611C>G ENSP00000450268.1:p.Thr204Ser
ENST00000550767.5:c.611C>G ENSP00000446637.1:p.Thr204Ser
NM_001270399.1:c.716C>G NP_001257328.1:p.Thr239Ser
NM_001270400.1:c.611C>G NP_001257329.1:p.Thr204Ser
NM_006009.3:c.716C>G NP_006000.2:p.Thr239Ser
NM_006009.4:c.716C>G MANE Select NP_006000.2:p.Thr239Ser
NM_001270399.2:c.716C>G NP_001257328.1:p.Thr239Ser
NM_001270400.2:c.611C>G NP_001257329.1:p.Thr204Ser