Canonical Allele Identifier: CA449777155

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30692042G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724265G>A , CM000668.2:g.30724265G>A	GRCh38
NC_000006.11:g.30692042G>A , CM000668.1:g.30692042G>A	GRCh37
NC_000006.10:g.30800021G>A	NCBI36
NG_034142.1:g.9065G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1203G>A MANE Select	ENSP00000339001.7:p.Glu401=
ENST00000680530.1:n.2065G>A
ENST00000681421.1:n.2269G>A
ENST00000681435.1:c.987G>A	ENSP00000506665.1:p.Glu329=
ENST00000327892.12:c.1203G>A	ENSP00000339001.7:p.Glu401=
ENST00000330914.7:c.987G>A	ENSP00000365578.2:p.Glu329=
ENST00000396384.1:c.987G>A	ENSP00000379668.1:p.Glu329=
ENST00000396389.5:c.1149G>A	ENSP00000379672.1:p.Glu383=
NM_001293212.1:c.1263G>A	NP_001280141.1:p.Glu421=
NM_001293213.1:c.597G>A	NP_001280142.1:p.Glu199=
NM_001293214.1:c.1071G>A	NP_001280143.1:p.Glu357=
NM_001293215.1:c.987G>A	NP_001280144.1:p.Glu329=
NM_001293216.1:c.987G>A	NP_001280145.1:p.Glu329=
NM_178014.3:c.1203G>A	NP_821133.1:p.Glu401=
NR_120608.1:n.910G>A
NM_178014.4:c.1203G>A MANE Select	NP_821133.1:p.Glu401=
NM_001293212.2:c.1263G>A	NP_001280141.1:p.Glu421=
NM_001293213.2:c.597G>A	NP_001280142.1:p.Glu199=
NM_001293214.2:c.1071G>A	NP_001280143.1:p.Glu357=
NM_001293215.2:c.987G>A	NP_001280144.1:p.Glu329=
NM_001293216.2:c.987G>A	NP_001280145.1:p.Glu329=
NR_120608.2:n.759G>A