Canonical Allele Identifier: CA363148648

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691635T>G (hg19) ; chr6:g.30723858T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723858T>G , CM000668.2:g.30723858T>G	GRCh38
NC_000006.11:g.30691635T>G , CM000668.1:g.30691635T>G	GRCh37
NC_000006.10:g.30799614T>G	NCBI36
NG_034142.1:g.8658T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.796T>G MANE Select	ENSP00000339001.7:p.Phe266Val
ENST00000680530.1:n.1658T>G
ENST00000681421.1:n.1862T>G
ENST00000681435.1:c.580T>G	ENSP00000506665.1:p.Phe194Val
ENST00000327892.12:c.796T>G	ENSP00000339001.7:p.Phe266Val
ENST00000330914.7:c.580T>G	ENSP00000365578.2:p.Phe194Val
ENST00000396384.1:c.580T>G	ENSP00000379668.1:p.Phe194Val
ENST00000396389.5:c.742T>G	ENSP00000379672.1:p.Phe248Val
NM_001293212.1:c.856T>G	NP_001280141.1:p.Phe286Val
NM_001293213.1:c.370-180T>G	NP_001280142.1:n.370-180T>G
NM_001293214.1:c.664T>G	NP_001280143.1:p.Phe222Val
NM_001293215.1:c.580T>G	NP_001280144.1:p.Phe194Val
NM_001293216.1:c.580T>G	NP_001280145.1:p.Phe194Val
NM_178014.3:c.796T>G	NP_821133.1:p.Phe266Val
NR_120608.1:n.584-81T>G
NM_178014.4:c.796T>G MANE Select	NP_821133.1:p.Phe266Val
NM_001293212.2:c.856T>G	NP_001280141.1:p.Phe286Val
NM_001293213.2:c.370-180T>G	NP_001280142.1:n.370-180T>G
NM_001293214.2:c.664T>G	NP_001280143.1:p.Phe222Val
NM_001293215.2:c.580T>G	NP_001280144.1:p.Phe194Val
NM_001293216.2:c.580T>G	NP_001280145.1:p.Phe194Val
NR_120608.2:n.433-81T>G