Canonical Allele Identifier: CA363148267

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691564T>A (hg19) ; chr6:g.30723787T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723787T>A , CM000668.2:g.30723787T>A	GRCh38
NC_000006.11:g.30691564T>A , CM000668.1:g.30691564T>A	GRCh37
NC_000006.10:g.30799543T>A	NCBI36
NG_034142.1:g.8587T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.725T>A MANE Select	ENSP00000339001.7:p.Phe242Tyr
ENST00000680530.1:n.1587T>A
ENST00000681421.1:n.1791T>A
ENST00000681435.1:c.509T>A	ENSP00000506665.1:p.Phe170Tyr
ENST00000327892.12:c.725T>A	ENSP00000339001.7:p.Phe242Tyr
ENST00000330914.7:c.509T>A	ENSP00000365578.2:p.Phe170Tyr
ENST00000396384.1:c.509T>A	ENSP00000379668.1:p.Phe170Tyr
ENST00000396389.5:c.671T>A	ENSP00000379672.1:p.Phe224Tyr
NM_001293212.1:c.785T>A	NP_001280141.1:p.Phe262Tyr
NM_001293213.1:c.370-251T>A	NP_001280142.1:n.370-251T>A
NM_001293214.1:c.593T>A	NP_001280143.1:p.Phe198Tyr
NM_001293215.1:c.509T>A	NP_001280144.1:p.Phe170Tyr
NM_001293216.1:c.509T>A	NP_001280145.1:p.Phe170Tyr
NM_178014.3:c.725T>A	NP_821133.1:p.Phe242Tyr
NR_120608.1:n.584-152T>A
NM_178014.4:c.725T>A MANE Select	NP_821133.1:p.Phe242Tyr
NM_001293212.2:c.785T>A	NP_001280141.1:p.Phe262Tyr
NM_001293213.2:c.370-251T>A	NP_001280142.1:n.370-251T>A
NM_001293214.2:c.593T>A	NP_001280143.1:p.Phe198Tyr
NM_001293215.2:c.509T>A	NP_001280144.1:p.Phe170Tyr
NM_001293216.2:c.509T>A	NP_001280145.1:p.Phe170Tyr
NR_120608.2:n.433-152T>A