Canonical Allele Identifier: CA363150693

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691932G>A (hg19) ; chr6:g.30724155G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724155G>A , CM000668.2:g.30724155G>A	GRCh38
NC_000006.11:g.30691932G>A , CM000668.1:g.30691932G>A	GRCh37
NC_000006.10:g.30799911G>A	NCBI36
NG_034142.1:g.8955G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1093G>A MANE Select	ENSP00000339001.7:p.Val365Ile
ENST00000680530.1:n.1955G>A
ENST00000681421.1:n.2159G>A
ENST00000681435.1:c.877G>A	ENSP00000506665.1:p.Val293Ile
ENST00000327892.12:c.1093G>A	ENSP00000339001.7:p.Val365Ile
ENST00000330914.7:c.877G>A	ENSP00000365578.2:p.Val293Ile
ENST00000396384.1:c.877G>A	ENSP00000379668.1:p.Val293Ile
ENST00000396389.5:c.1039G>A	ENSP00000379672.1:p.Val347Ile
NM_001293212.1:c.1153G>A	NP_001280141.1:p.Val385Ile
NM_001293213.1:c.487G>A	NP_001280142.1:p.Val163Ile
NM_001293214.1:c.961G>A	NP_001280143.1:p.Val321Ile
NM_001293215.1:c.877G>A	NP_001280144.1:p.Val293Ile
NM_001293216.1:c.877G>A	NP_001280145.1:p.Val293Ile
NM_178014.3:c.1093G>A	NP_821133.1:p.Val365Ile
NR_120608.1:n.800G>A
NM_178014.4:c.1093G>A MANE Select	NP_821133.1:p.Val365Ile
NM_001293212.2:c.1153G>A	NP_001280141.1:p.Val385Ile
NM_001293213.2:c.487G>A	NP_001280142.1:p.Val163Ile
NM_001293214.2:c.961G>A	NP_001280143.1:p.Val321Ile
NM_001293215.2:c.877G>A	NP_001280144.1:p.Val293Ile
NM_001293216.2:c.877G>A	NP_001280145.1:p.Val293Ile
NR_120608.2:n.649G>A