Canonical Allele Identifier: CA384645701

Gene: TUBA1A

Linked Data

• ClinVar Variation Id: 432052
• ClinVar RCV Id: RCV000498733 ; RCV000767452 ; RCV001253098
• dbSNP Id: rs1555162549
• MyVariant Identifiers: chr12:g.49580538G>A (hg19) ; chr12:g.49186755G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49186755G>A , CM000674.2:g.49186755G>A	GRCh38
NC_000012.11:g.49580538G>A , CM000674.1:g.49580538G>A	GRCh37
NC_000012.10:g.47866805G>A	NCBI36
NG_008966.1:g.7324C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.82C>T MANE Select	ENSP00000301071.7:p.His28Tyr
ENST00000547939.6:c.-24C>T	ENSP00000450268.2:n.-24C>T
ENST00000550767.6:c.-24C>T	ENSP00000446637.1:n.-24C>T
ENST00000550811.2:n.1115C>T
ENST00000552924.2:c.-24C>T	ENSP00000448725.2:n.-24C>T
ENST00000679733.1:c.82C>T	ENSP00000505459.1:p.His28Tyr
ENST00000295766.9:c.82C>T	ENSP00000439020.2:p.His28Tyr
ENST00000301071.11:c.82C>T	ENSP00000301071.7:p.His28Tyr
ENST00000546918.1:c.82C>T	ENSP00000446613.1:p.His28Tyr
ENST00000547939.5:c.-24C>T	ENSP00000450268.1:n.-24C>T
ENST00000548363.1:n.86C>T
ENST00000550254.1:n.104C>T
ENST00000550767.5:c.-24C>T	ENSP00000446637.1:n.-24C>T
ENST00000550811.1:c.-24C>T	ENSP00000449016.1:n.-24C>T
ENST00000552924.1:c.-24C>T	ENSP00000448725.1:n.-24C>T
NM_001270399.1:c.82C>T	NP_001257328.1:p.His28Tyr
NM_001270400.1:c.-24C>T	NP_001257329.1:n.-24C>T
NM_006009.3:c.82C>T	NP_006000.2:p.His28Tyr
NM_006009.4:c.82C>T MANE Select	NP_006000.2:p.His28Tyr
NM_001270399.2:c.82C>T	NP_001257328.1:p.His28Tyr
NM_001270400.2:c.-24C>T	NP_001257329.1:n.-24C>T