Canonical Allele Identifier: CA363149073

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691737A>G (hg19) ; chr6:g.30723960A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723960A>G , CM000668.2:g.30723960A>G	GRCh38
NC_000006.11:g.30691737A>G , CM000668.1:g.30691737A>G	GRCh37
NC_000006.10:g.30799716A>G	NCBI36
NG_034142.1:g.8760A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.898A>G MANE Select	ENSP00000339001.7:p.Met300Val
ENST00000680530.1:n.1760A>G
ENST00000681421.1:n.1964A>G
ENST00000681435.1:c.682A>G	ENSP00000506665.1:p.Met228Val
ENST00000327892.12:c.898A>G	ENSP00000339001.7:p.Met300Val
ENST00000330914.7:c.682A>G	ENSP00000365578.2:p.Met228Val
ENST00000396384.1:c.682A>G	ENSP00000379668.1:p.Met228Val
ENST00000396389.5:c.844A>G	ENSP00000379672.1:p.Met282Val
NM_001293212.1:c.958A>G	NP_001280141.1:p.Met320Val
NM_001293213.1:c.370-78A>G	NP_001280142.1:n.370-78A>G
NM_001293214.1:c.766A>G	NP_001280143.1:p.Met256Val
NM_001293215.1:c.682A>G	NP_001280144.1:p.Met228Val
NM_001293216.1:c.682A>G	NP_001280145.1:p.Met228Val
NM_178014.3:c.898A>G	NP_821133.1:p.Met300Val
NR_120608.1:n.605A>G
NM_178014.4:c.898A>G MANE Select	NP_821133.1:p.Met300Val
NM_001293212.2:c.958A>G	NP_001280141.1:p.Met320Val
NM_001293213.2:c.370-78A>G	NP_001280142.1:n.370-78A>G
NM_001293214.2:c.766A>G	NP_001280143.1:p.Met256Val
NM_001293215.2:c.682A>G	NP_001280144.1:p.Met228Val
NM_001293216.2:c.682A>G	NP_001280145.1:p.Met228Val
NR_120608.2:n.454A>G