Canonical Allele Identifier: CA363151814

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30692095T>A (hg19) ; chr6:g.30724318T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724318T>A , CM000668.2:g.30724318T>A	GRCh38
NC_000006.11:g.30692095T>A , CM000668.1:g.30692095T>A	GRCh37
NC_000006.10:g.30800074T>A	NCBI36
NG_034142.1:g.9118T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1256T>A MANE Select	ENSP00000339001.7:p.Val419Asp
ENST00000680530.1:n.2118T>A
ENST00000681421.1:n.2322T>A
ENST00000681435.1:c.1040T>A	ENSP00000506665.1:p.Val347Asp
ENST00000327892.12:c.1256T>A	ENSP00000339001.7:p.Val419Asp
ENST00000330914.7:c.1040T>A	ENSP00000365578.2:p.Val347Asp
ENST00000396384.1:c.1040T>A	ENSP00000379668.1:p.Val347Asp
ENST00000396389.5:c.1202T>A	ENSP00000379672.1:p.Val401Asp
NM_001293212.1:c.1316T>A	NP_001280141.1:p.Val439Asp
NM_001293213.1:c.650T>A	NP_001280142.1:p.Val217Asp
NM_001293214.1:c.1124T>A	NP_001280143.1:p.Val375Asp
NM_001293215.1:c.1040T>A	NP_001280144.1:p.Val347Asp
NM_001293216.1:c.1040T>A	NP_001280145.1:p.Val347Asp
NM_178014.3:c.1256T>A	NP_821133.1:p.Val419Asp
NR_120608.1:n.963T>A
NM_178014.4:c.1256T>A MANE Select	NP_821133.1:p.Val419Asp
NM_001293212.2:c.1316T>A	NP_001280141.1:p.Val439Asp
NM_001293213.2:c.650T>A	NP_001280142.1:p.Val217Asp
NM_001293214.2:c.1124T>A	NP_001280143.1:p.Val375Asp
NM_001293215.2:c.1040T>A	NP_001280144.1:p.Val347Asp
NM_001293216.2:c.1040T>A	NP_001280145.1:p.Val347Asp
NR_120608.2:n.812T>A