Canonical Allele Identifier: CA213277

Gene: TUBA1A

Linked Data

• ClinVar Variation Id: 160163
• ClinVar RCV Id: RCV000147817
• dbSNP Id: rs587784493
• MyVariant Identifiers: chr12:g.49579391G>C (hg19) ; chr12:g.49185608G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185608G>C , CM000674.2:g.49185608G>C	GRCh38
NC_000012.11:g.49579391G>C , CM000674.1:g.49579391G>C	GRCh37
NC_000012.10:g.47865658G>C	NCBI36
NG_008966.1:g.8471C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.758C>G MANE Select	ENSP00000301071.7:p.Thr253Arg
ENST00000547939.6:c.653C>G	ENSP00000450268.2:p.Thr218Arg
ENST00000550767.6:c.653C>G	ENSP00000446637.1:p.Thr218Arg
ENST00000550811.2:n.1791C>G
ENST00000552924.2:c.653C>G	ENSP00000448725.2:p.Thr218Arg
ENST00000679733.1:c.*214C>G	ENSP00000505459.1:n.*214C>G
ENST00000295766.9:c.758C>G	ENSP00000439020.2:p.Thr253Arg
ENST00000301071.11:c.758C>G	ENSP00000301071.7:p.Thr253Arg
ENST00000547939.5:c.653C>G	ENSP00000450268.1:p.Thr218Arg
ENST00000550767.5:c.653C>G	ENSP00000446637.1:p.Thr218Arg
NM_001270399.1:c.758C>G	NP_001257328.1:p.Thr253Arg
NM_001270400.1:c.653C>G	NP_001257329.1:p.Thr218Arg
NM_006009.3:c.758C>G	NP_006000.2:p.Thr253Arg
NM_006009.4:c.758C>G MANE Select	NP_006000.2:p.Thr253Arg
NM_001270399.2:c.758C>G	NP_001257328.1:p.Thr253Arg
NM_001270400.2:c.653C>G	NP_001257329.1:p.Thr218Arg