Canonical Allele Identifier: CA384639505

Gene: TUBA1A

Linked Data

• ClinVar Variation Id: 1339565
• ClinVar RCV Id: RCV001824274
• dbSNP Id: rs2121243396
• MyVariant Identifiers: chr12:g.49579331G>T (hg19) ; chr12:g.49185548G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185548G>T , CM000674.2:g.49185548G>T	GRCh38
NC_000012.11:g.49579331G>T , CM000674.1:g.49579331G>T	GRCh37
NC_000012.10:g.47865598G>T	NCBI36
NG_008966.1:g.8531C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.818C>A MANE Select	ENSP00000301071.7:p.Ala273Asp
ENST00000547939.6:c.713C>A	ENSP00000450268.2:p.Ala238Asp
ENST00000550767.6:c.713C>A	ENSP00000446637.1:p.Ala238Asp
ENST00000550811.2:n.1851C>A
ENST00000552924.2:c.713C>A	ENSP00000448725.2:p.Ala238Asp
ENST00000679733.1:c.*274C>A	ENSP00000505459.1:n.*274C>A
ENST00000295766.9:c.818C>A	ENSP00000439020.2:p.Ala273Asp
ENST00000301071.11:c.818C>A	ENSP00000301071.7:p.Ala273Asp
ENST00000550767.5:c.713C>A	ENSP00000446637.1:p.Ala238Asp
NM_001270399.1:c.818C>A	NP_001257328.1:p.Ala273Asp
NM_001270400.1:c.713C>A	NP_001257329.1:p.Ala238Asp
NM_006009.3:c.818C>A	NP_006000.2:p.Ala273Asp
NM_006009.4:c.818C>A MANE Select	NP_006000.2:p.Ala273Asp
NM_001270399.2:c.818C>A	NP_001257328.1:p.Ala273Asp
NM_001270400.2:c.713C>A	NP_001257329.1:p.Ala238Asp