Canonical Allele Identifier: CA384639660

Gene: TUBA1A

Linked Data

• MyVariant Identifiers: chr12:g.49579350A>C (hg19) ; chr12:g.49185567A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185567A>C , CM000674.2:g.49185567A>C	GRCh38
NC_000012.11:g.49579350A>C , CM000674.1:g.49579350A>C	GRCh37
NC_000012.10:g.47865617A>C	NCBI36
NG_008966.1:g.8512T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.799T>G MANE Select	ENSP00000301071.7:p.Phe267Val
ENST00000547939.6:c.694T>G	ENSP00000450268.2:p.Phe232Val
ENST00000550767.6:c.694T>G	ENSP00000446637.1:p.Phe232Val
ENST00000550811.2:n.1832T>G
ENST00000552924.2:c.694T>G	ENSP00000448725.2:p.Phe232Val
ENST00000679733.1:c.*255T>G	ENSP00000505459.1:n.*255T>G
ENST00000295766.9:c.799T>G	ENSP00000439020.2:p.Phe267Val
ENST00000301071.11:c.799T>G	ENSP00000301071.7:p.Phe267Val
ENST00000550767.5:c.694T>G	ENSP00000446637.1:p.Phe232Val
NM_001270399.1:c.799T>G	NP_001257328.1:p.Phe267Val
NM_001270400.1:c.694T>G	NP_001257329.1:p.Phe232Val
NM_006009.3:c.799T>G	NP_006000.2:p.Phe267Val
NM_006009.4:c.799T>G MANE Select	NP_006000.2:p.Phe267Val
NM_001270399.2:c.799T>G	NP_001257328.1:p.Phe267Val
NM_001270400.2:c.694T>G	NP_001257329.1:p.Phe232Val