Canonical Allele Identifier: CA16619549
Gene: TUBA1A HGNC NCBI

Linked Data

ClinVar Variation Id: 421873
ClinVar RCV Id: RCV000486639 RCV000767450
dbSNP Id: rs1064795417
MyVariant Identifiers: chr12:g.49579334T>C (hg19) chr12:g.49185551T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49185551T>C , CM000674.2:g.49185551T>C GRCh38
NC_000012.11:g.49579334T>C , CM000674.1:g.49579334T>C GRCh37
NC_000012.10:g.47865601T>C NCBI36
NG_008966.1:g.8528A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000301071.12:c.815A>G MANE Select ENSP00000301071.7:p.Tyr272Cys
ENST00000547939.6:c.710A>G ENSP00000450268.2:p.Tyr237Cys
ENST00000550767.6:c.710A>G ENSP00000446637.1:p.Tyr237Cys
ENST00000550811.2:n.1848A>G
ENST00000552924.2:c.710A>G ENSP00000448725.2:p.Tyr237Cys
ENST00000679733.1:c.*271A>G ENSP00000505459.1:n.*271A>G
ENST00000295766.9:c.815A>G ENSP00000439020.2:p.Tyr272Cys
ENST00000301071.11:c.815A>G ENSP00000301071.7:p.Tyr272Cys
ENST00000550767.5:c.710A>G ENSP00000446637.1:p.Tyr237Cys
NM_001270399.1:c.815A>G NP_001257328.1:p.Tyr272Cys
NM_001270400.1:c.710A>G NP_001257329.1:p.Tyr237Cys
NM_006009.3:c.815A>G NP_006000.2:p.Tyr272Cys
NM_006009.4:c.815A>G MANE Select NP_006000.2:p.Tyr272Cys
NM_001270399.2:c.815A>G NP_001257328.1:p.Tyr272Cys
NM_001270400.2:c.710A>G NP_001257329.1:p.Tyr237Cys
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