Canonical Allele Identifier: CA384641862

Gene: TUBA1A

Linked Data

• ClinVar Variation Id: 2583182
• ClinVar RCV Id: RCV003334473
• MyVariant Identifiers: chr12:g.49579608C>T (hg19) ; chr12:g.49185825C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185825C>T , CM000674.2:g.49185825C>T	GRCh38
NC_000012.11:g.49579608C>T , CM000674.1:g.49579608C>T	GRCh37
NC_000012.10:g.47865875C>T	NCBI36
NG_008966.1:g.8254G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.541G>A MANE Select	ENSP00000301071.7:p.Val181Ile
ENST00000547939.6:c.436G>A	ENSP00000450268.2:p.Val146Ile
ENST00000550767.6:c.436G>A	ENSP00000446637.1:p.Val146Ile
ENST00000550811.2:n.1574G>A
ENST00000552924.2:c.436G>A	ENSP00000448725.2:p.Val146Ile
ENST00000679733.1:c.564G>A	ENSP00000505459.1:p.Leu188=
ENST00000295766.9:c.541G>A	ENSP00000439020.2:p.Val181Ile
ENST00000301071.11:c.541G>A	ENSP00000301071.7:p.Val181Ile
ENST00000546918.1:c.693G>A	ENSP00000446613.1:p.Leu231=
ENST00000547939.5:c.436G>A	ENSP00000450268.1:p.Val146Ile
ENST00000550767.5:c.436G>A	ENSP00000446637.1:p.Val146Ile
NM_001270399.1:c.541G>A	NP_001257328.1:p.Val181Ile
NM_001270400.1:c.436G>A	NP_001257329.1:p.Val146Ile
NM_006009.3:c.541G>A	NP_006000.2:p.Val181Ile
NM_006009.4:c.541G>A MANE Select	NP_006000.2:p.Val181Ile
NM_001270399.2:c.541G>A	NP_001257328.1:p.Val181Ile
NM_001270400.2:c.436G>A	NP_001257329.1:p.Val146Ile