Canonical Allele Identifier: CA449776963

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691916T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724139T>G , CM000668.2:g.30724139T>G	GRCh38
NC_000006.11:g.30691916T>G , CM000668.1:g.30691916T>G	GRCh37
NC_000006.10:g.30799895T>G	NCBI36
NG_034142.1:g.8939T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1077T>G MANE Select	ENSP00000339001.7:p.Arg359=
ENST00000680530.1:n.1939T>G
ENST00000681421.1:n.2143T>G
ENST00000681435.1:c.861T>G	ENSP00000506665.1:p.Arg287=
ENST00000327892.12:c.1077T>G	ENSP00000339001.7:p.Arg359=
ENST00000330914.7:c.861T>G	ENSP00000365578.2:p.Arg287=
ENST00000396384.1:c.861T>G	ENSP00000379668.1:p.Arg287=
ENST00000396389.5:c.1023T>G	ENSP00000379672.1:p.Arg341=
NM_001293212.1:c.1137T>G	NP_001280141.1:p.Arg379=
NM_001293213.1:c.471T>G	NP_001280142.1:p.Arg157=
NM_001293214.1:c.945T>G	NP_001280143.1:p.Arg315=
NM_001293215.1:c.861T>G	NP_001280144.1:p.Arg287=
NM_001293216.1:c.861T>G	NP_001280145.1:p.Arg287=
NM_178014.3:c.1077T>G	NP_821133.1:p.Arg359=
NR_120608.1:n.784T>G
NM_178014.4:c.1077T>G MANE Select	NP_821133.1:p.Arg359=
NM_001293212.2:c.1137T>G	NP_001280141.1:p.Arg379=
NM_001293213.2:c.471T>G	NP_001280142.1:p.Arg157=
NM_001293214.2:c.945T>G	NP_001280143.1:p.Arg315=
NM_001293215.2:c.861T>G	NP_001280144.1:p.Arg287=
NM_001293216.2:c.861T>G	NP_001280145.1:p.Arg287=
NR_120608.2:n.633T>G