Canonical Allele Identifier: CA363151573

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30692055A>G (hg19) ; chr6:g.30724278A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724278A>G , CM000668.2:g.30724278A>G	GRCh38
NC_000006.11:g.30692055A>G , CM000668.1:g.30692055A>G	GRCh37
NC_000006.10:g.30800034A>G	NCBI36
NG_034142.1:g.9078A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1216A>G MANE Select	ENSP00000339001.7:p.Met406Val
ENST00000680530.1:n.2078A>G
ENST00000681421.1:n.2282A>G
ENST00000681435.1:c.1000A>G	ENSP00000506665.1:p.Met334Val
ENST00000327892.12:c.1216A>G	ENSP00000339001.7:p.Met406Val
ENST00000330914.7:c.1000A>G	ENSP00000365578.2:p.Met334Val
ENST00000396384.1:c.1000A>G	ENSP00000379668.1:p.Met334Val
ENST00000396389.5:c.1162A>G	ENSP00000379672.1:p.Met388Val
NM_001293212.1:c.1276A>G	NP_001280141.1:p.Met426Val
NM_001293213.1:c.610A>G	NP_001280142.1:p.Met204Val
NM_001293214.1:c.1084A>G	NP_001280143.1:p.Met362Val
NM_001293215.1:c.1000A>G	NP_001280144.1:p.Met334Val
NM_001293216.1:c.1000A>G	NP_001280145.1:p.Met334Val
NM_178014.3:c.1216A>G	NP_821133.1:p.Met406Val
NR_120608.1:n.923A>G
NM_178014.4:c.1216A>G MANE Select	NP_821133.1:p.Met406Val
NM_001293212.2:c.1276A>G	NP_001280141.1:p.Met426Val
NM_001293213.2:c.610A>G	NP_001280142.1:p.Met204Val
NM_001293214.2:c.1084A>G	NP_001280143.1:p.Met362Val
NM_001293215.2:c.1000A>G	NP_001280144.1:p.Met334Val
NM_001293216.2:c.1000A>G	NP_001280145.1:p.Met334Val
NR_120608.2:n.772A>G