Canonical Allele Identifier: CA363149408

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691780C>T (hg19) ; chr6:g.30724003C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724003C>T , CM000668.2:g.30724003C>T	GRCh38
NC_000006.11:g.30691780C>T , CM000668.1:g.30691780C>T	GRCh37
NC_000006.10:g.30799759C>T	NCBI36
NG_034142.1:g.8803C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.941C>T MANE Select	ENSP00000339001.7:p.Ala314Val
ENST00000680530.1:n.1803C>T
ENST00000681421.1:n.2007C>T
ENST00000681435.1:c.725C>T	ENSP00000506665.1:p.Ala242Val
ENST00000327892.12:c.941C>T	ENSP00000339001.7:p.Ala314Val
ENST00000330914.7:c.725C>T	ENSP00000365578.2:p.Ala242Val
ENST00000396384.1:c.725C>T	ENSP00000379668.1:p.Ala242Val
ENST00000396389.5:c.887C>T	ENSP00000379672.1:p.Ala296Val
NM_001293212.1:c.1001C>T	NP_001280141.1:p.Ala334Val
NM_001293213.1:c.370-35C>T	NP_001280142.1:n.370-35C>T
NM_001293214.1:c.809C>T	NP_001280143.1:p.Ala270Val
NM_001293215.1:c.725C>T	NP_001280144.1:p.Ala242Val
NM_001293216.1:c.725C>T	NP_001280145.1:p.Ala242Val
NM_178014.3:c.941C>T	NP_821133.1:p.Ala314Val
NR_120608.1:n.648C>T
NM_178014.4:c.941C>T MANE Select	NP_821133.1:p.Ala314Val
NM_001293212.2:c.1001C>T	NP_001280141.1:p.Ala334Val
NM_001293213.2:c.370-35C>T	NP_001280142.1:n.370-35C>T
NM_001293214.2:c.809C>T	NP_001280143.1:p.Ala270Val
NM_001293215.2:c.725C>T	NP_001280144.1:p.Ala242Val
NM_001293216.2:c.725C>T	NP_001280145.1:p.Ala242Val
NR_120608.2:n.497C>T