Canonical Allele Identifier: CA363151652

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30692068A>T (hg19) ; chr6:g.30724291A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724291A>T , CM000668.2:g.30724291A>T	GRCh38
NC_000006.11:g.30692068A>T , CM000668.1:g.30692068A>T	GRCh37
NC_000006.10:g.30800047A>T	NCBI36
NG_034142.1:g.9091A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1229A>T MANE Select	ENSP00000339001.7:p.Glu410Val
ENST00000680530.1:n.2091A>T
ENST00000681421.1:n.2295A>T
ENST00000681435.1:c.1013A>T	ENSP00000506665.1:p.Glu338Val
ENST00000327892.12:c.1229A>T	ENSP00000339001.7:p.Glu410Val
ENST00000330914.7:c.1013A>T	ENSP00000365578.2:p.Glu338Val
ENST00000396384.1:c.1013A>T	ENSP00000379668.1:p.Glu338Val
ENST00000396389.5:c.1175A>T	ENSP00000379672.1:p.Glu392Val
NM_001293212.1:c.1289A>T	NP_001280141.1:p.Glu430Val
NM_001293213.1:c.623A>T	NP_001280142.1:p.Glu208Val
NM_001293214.1:c.1097A>T	NP_001280143.1:p.Glu366Val
NM_001293215.1:c.1013A>T	NP_001280144.1:p.Glu338Val
NM_001293216.1:c.1013A>T	NP_001280145.1:p.Glu338Val
NM_178014.3:c.1229A>T	NP_821133.1:p.Glu410Val
NR_120608.1:n.936A>T
NM_178014.4:c.1229A>T MANE Select	NP_821133.1:p.Glu410Val
NM_001293212.2:c.1289A>T	NP_001280141.1:p.Glu430Val
NM_001293213.2:c.623A>T	NP_001280142.1:p.Glu208Val
NM_001293214.2:c.1097A>T	NP_001280143.1:p.Glu366Val
NM_001293215.2:c.1013A>T	NP_001280144.1:p.Glu338Val
NM_001293216.2:c.1013A>T	NP_001280145.1:p.Glu338Val
NR_120608.2:n.785A>T