Canonical Allele Identifier: CA363150133

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691860T>A (hg19) ; chr6:g.30724083T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724083T>A , CM000668.2:g.30724083T>A	GRCh38
NC_000006.11:g.30691860T>A , CM000668.1:g.30691860T>A	GRCh37
NC_000006.10:g.30799839T>A	NCBI36
NG_034142.1:g.8883T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1021T>A MANE Select	ENSP00000339001.7:p.Phe341Ile
ENST00000680530.1:n.1883T>A
ENST00000681421.1:n.2087T>A
ENST00000681435.1:c.805T>A	ENSP00000506665.1:p.Phe269Ile
ENST00000327892.12:c.1021T>A	ENSP00000339001.7:p.Phe341Ile
ENST00000330914.7:c.805T>A	ENSP00000365578.2:p.Phe269Ile
ENST00000396384.1:c.805T>A	ENSP00000379668.1:p.Phe269Ile
ENST00000396389.5:c.967T>A	ENSP00000379672.1:p.Phe323Ile
NM_001293212.1:c.1081T>A	NP_001280141.1:p.Phe361Ile
NM_001293213.1:c.415T>A	NP_001280142.1:p.Phe139Ile
NM_001293214.1:c.889T>A	NP_001280143.1:p.Phe297Ile
NM_001293215.1:c.805T>A	NP_001280144.1:p.Phe269Ile
NM_001293216.1:c.805T>A	NP_001280145.1:p.Phe269Ile
NM_178014.3:c.1021T>A	NP_821133.1:p.Phe341Ile
NR_120608.1:n.728T>A
NM_178014.4:c.1021T>A MANE Select	NP_821133.1:p.Phe341Ile
NM_001293212.2:c.1081T>A	NP_001280141.1:p.Phe361Ile
NM_001293213.2:c.415T>A	NP_001280142.1:p.Phe139Ile
NM_001293214.2:c.889T>A	NP_001280143.1:p.Phe297Ile
NM_001293215.2:c.805T>A	NP_001280144.1:p.Phe269Ile
NM_001293216.2:c.805T>A	NP_001280145.1:p.Phe269Ile
NR_120608.2:n.577T>A