Canonical Allele Identifier: CA363148562

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691617T>G (hg19) ; chr6:g.30723840T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723840T>G , CM000668.2:g.30723840T>G	GRCh38
NC_000006.11:g.30691617T>G , CM000668.1:g.30691617T>G	GRCh37
NC_000006.10:g.30799596T>G	NCBI36
NG_034142.1:g.8640T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.778T>G MANE Select	ENSP00000339001.7:p.Phe260Val
ENST00000680530.1:n.1640T>G
ENST00000681421.1:n.1844T>G
ENST00000681435.1:c.562T>G	ENSP00000506665.1:p.Phe188Val
ENST00000327892.12:c.778T>G	ENSP00000339001.7:p.Phe260Val
ENST00000330914.7:c.562T>G	ENSP00000365578.2:p.Phe188Val
ENST00000396384.1:c.562T>G	ENSP00000379668.1:p.Phe188Val
ENST00000396389.5:c.724T>G	ENSP00000379672.1:p.Phe242Val
NM_001293212.1:c.838T>G	NP_001280141.1:p.Phe280Val
NM_001293213.1:c.370-198T>G	NP_001280142.1:n.370-198T>G
NM_001293214.1:c.646T>G	NP_001280143.1:p.Phe216Val
NM_001293215.1:c.562T>G	NP_001280144.1:p.Phe188Val
NM_001293216.1:c.562T>G	NP_001280145.1:p.Phe188Val
NM_178014.3:c.778T>G	NP_821133.1:p.Phe260Val
NR_120608.1:n.584-99T>G
NM_178014.4:c.778T>G MANE Select	NP_821133.1:p.Phe260Val
NM_001293212.2:c.838T>G	NP_001280141.1:p.Phe280Val
NM_001293213.2:c.370-198T>G	NP_001280142.1:n.370-198T>G
NM_001293214.2:c.646T>G	NP_001280143.1:p.Phe216Val
NM_001293215.2:c.562T>G	NP_001280144.1:p.Phe188Val
NM_001293216.2:c.562T>G	NP_001280145.1:p.Phe188Val
NR_120608.2:n.433-99T>G