Canonical Allele Identifier: CA363150724

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691938T>G (hg19) ; chr6:g.30724161T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724161T>G , CM000668.2:g.30724161T>G	GRCh38
NC_000006.11:g.30691938T>G , CM000668.1:g.30691938T>G	GRCh37
NC_000006.10:g.30799917T>G	NCBI36
NG_034142.1:g.8961T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1099T>G MANE Select	ENSP00000339001.7:p.Phe367Val
ENST00000680530.1:n.1961T>G
ENST00000681421.1:n.2165T>G
ENST00000681435.1:c.883T>G	ENSP00000506665.1:p.Phe295Val
ENST00000327892.12:c.1099T>G	ENSP00000339001.7:p.Phe367Val
ENST00000330914.7:c.883T>G	ENSP00000365578.2:p.Phe295Val
ENST00000396384.1:c.883T>G	ENSP00000379668.1:p.Phe295Val
ENST00000396389.5:c.1045T>G	ENSP00000379672.1:p.Phe349Val
NM_001293212.1:c.1159T>G	NP_001280141.1:p.Phe387Val
NM_001293213.1:c.493T>G	NP_001280142.1:p.Phe165Val
NM_001293214.1:c.967T>G	NP_001280143.1:p.Phe323Val
NM_001293215.1:c.883T>G	NP_001280144.1:p.Phe295Val
NM_001293216.1:c.883T>G	NP_001280145.1:p.Phe295Val
NM_178014.3:c.1099T>G	NP_821133.1:p.Phe367Val
NR_120608.1:n.806T>G
NM_178014.4:c.1099T>G MANE Select	NP_821133.1:p.Phe367Val
NM_001293212.2:c.1159T>G	NP_001280141.1:p.Phe387Val
NM_001293213.2:c.493T>G	NP_001280142.1:p.Phe165Val
NM_001293214.2:c.967T>G	NP_001280143.1:p.Phe323Val
NM_001293215.2:c.883T>G	NP_001280144.1:p.Phe295Val
NM_001293216.2:c.883T>G	NP_001280145.1:p.Phe295Val
NR_120608.2:n.655T>G