Canonical Allele Identifier: CA384634490
Community Standard Title: NM_006009.4(TUBA1A):c.1222T>G (p.Tyr408Asp)
Gene: TUBA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49185144A>C , CM000674.2:g.49185144A>C GRCh38
NC_000012.11:g.49578927A>C , CM000674.1:g.49578927A>C GRCh37
NC_000012.10:g.47865194A>C NCBI36
NG_008966.1:g.8935T>G

Transcript Alleles

HGVS Amino-acid Change
NM_006009.4:c.1222T>G MANE Select NP_006000.2:p.Tyr408Asp
ENST00000301071.12:c.1222T>G MANE Select ENSP00000301071.7:p.Tyr408Asp
NM_001270399.1:c.1222T>G NP_001257328.1:p.Tyr408Asp
NM_001270399.2:c.1222T>G NP_001257328.1:p.Tyr408Asp
NM_001270400.1:c.1117T>G NP_001257329.1:p.Tyr373Asp
NM_001270400.2:c.1117T>G NP_001257329.1:p.Tyr373Asp
NM_006009.3:c.1222T>G NP_006000.2:p.Tyr408Asp
ENST00000295766.9:c.1222T>G ENSP00000439020.2:p.Tyr408Asp
ENST00000301071.11:c.1222T>G ENSP00000301071.7:p.Tyr408Asp
ENST00000547939.6:c.1117T>G ENSP00000450268.2:p.Tyr373Asp
ENST00000550767.5:c.1117T>G ENSP00000446637.1:p.Tyr373Asp
ENST00000550767.6:c.1117T>G ENSP00000446637.1:p.Tyr373Asp
ENST00000550811.2:n.2255T>G
ENST00000552924.2:c.1117T>G ENSP00000448725.2:p.Tyr373Asp
ENST00000679733.1:c.*678T>G ENSP00000505459.1:n.*678T>G