Canonical Allele Identifier: CA384640130

Gene: TUBA1A

Linked Data

• ClinVar Variation Id: 864865
• ClinVar RCV Id: RCV001072148
• dbSNP Id: rs1942171146
• MyVariant Identifiers: chr12:g.49579403T>C (hg19) ; chr12:g.49185620T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185620T>C , CM000674.2:g.49185620T>C	GRCh38
NC_000012.11:g.49579403T>C , CM000674.1:g.49579403T>C	GRCh37
NC_000012.10:g.47865670T>C	NCBI36
NG_008966.1:g.8459A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.746A>G MANE Select	ENSP00000301071.7:p.Asn249Ser
ENST00000547939.6:c.641A>G	ENSP00000450268.2:p.Asn214Ser
ENST00000550767.6:c.641A>G	ENSP00000446637.1:p.Asn214Ser
ENST00000550811.2:n.1779A>G
ENST00000552924.2:c.641A>G	ENSP00000448725.2:p.Asn214Ser
ENST00000679733.1:c.*202A>G	ENSP00000505459.1:n.*202A>G
ENST00000295766.9:c.746A>G	ENSP00000439020.2:p.Asn249Ser
ENST00000301071.11:c.746A>G	ENSP00000301071.7:p.Asn249Ser
ENST00000547939.5:c.641A>G	ENSP00000450268.1:p.Asn214Ser
ENST00000550767.5:c.641A>G	ENSP00000446637.1:p.Asn214Ser
NM_001270399.1:c.746A>G	NP_001257328.1:p.Asn249Ser
NM_001270400.1:c.641A>G	NP_001257329.1:p.Asn214Ser
NM_006009.3:c.746A>G	NP_006000.2:p.Asn249Ser
NM_006009.4:c.746A>G MANE Select	NP_006000.2:p.Asn249Ser
NM_001270399.2:c.746A>G	NP_001257328.1:p.Asn249Ser
NM_001270400.2:c.641A>G	NP_001257329.1:p.Asn214Ser