Canonical Allele Identifier: CA363150910

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691957C>T (hg19) ; chr6:g.30724180C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724180C>T , CM000668.2:g.30724180C>T	GRCh38
NC_000006.11:g.30691957C>T , CM000668.1:g.30691957C>T	GRCh37
NC_000006.10:g.30799936C>T	NCBI36
NG_034142.1:g.8980C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1118C>T MANE Select	ENSP00000339001.7:p.Ala373Val
ENST00000680530.1:n.1980C>T
ENST00000681421.1:n.2184C>T
ENST00000681435.1:c.902C>T	ENSP00000506665.1:p.Ala301Val
ENST00000327892.12:c.1118C>T	ENSP00000339001.7:p.Ala373Val
ENST00000330914.7:c.902C>T	ENSP00000365578.2:p.Ala301Val
ENST00000396384.1:c.902C>T	ENSP00000379668.1:p.Ala301Val
ENST00000396389.5:c.1064C>T	ENSP00000379672.1:p.Ala355Val
NM_001293212.1:c.1178C>T	NP_001280141.1:p.Ala393Val
NM_001293213.1:c.512C>T	NP_001280142.1:p.Ala171Val
NM_001293214.1:c.986C>T	NP_001280143.1:p.Ala329Val
NM_001293215.1:c.902C>T	NP_001280144.1:p.Ala301Val
NM_001293216.1:c.902C>T	NP_001280145.1:p.Ala301Val
NM_178014.3:c.1118C>T	NP_821133.1:p.Ala373Val
NR_120608.1:n.825C>T
NM_178014.4:c.1118C>T MANE Select	NP_821133.1:p.Ala373Val
NM_001293212.2:c.1178C>T	NP_001280141.1:p.Ala393Val
NM_001293213.2:c.512C>T	NP_001280142.1:p.Ala171Val
NM_001293214.2:c.986C>T	NP_001280143.1:p.Ala329Val
NM_001293215.2:c.902C>T	NP_001280144.1:p.Ala301Val
NM_001293216.2:c.902C>T	NP_001280145.1:p.Ala301Val
NR_120608.2:n.674C>T