Canonical Allele Identifier: CA363148661

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691638A>G (hg19) ; chr6:g.30723861A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723861A>G , CM000668.2:g.30723861A>G	GRCh38
NC_000006.11:g.30691638A>G , CM000668.1:g.30691638A>G	GRCh37
NC_000006.10:g.30799617A>G	NCBI36
NG_034142.1:g.8661A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.799A>G MANE Select	ENSP00000339001.7:p.Met267Val
ENST00000680530.1:n.1661A>G
ENST00000681421.1:n.1865A>G
ENST00000681435.1:c.583A>G	ENSP00000506665.1:p.Met195Val
ENST00000327892.12:c.799A>G	ENSP00000339001.7:p.Met267Val
ENST00000330914.7:c.583A>G	ENSP00000365578.2:p.Met195Val
ENST00000396384.1:c.583A>G	ENSP00000379668.1:p.Met195Val
ENST00000396389.5:c.745A>G	ENSP00000379672.1:p.Met249Val
NM_001293212.1:c.859A>G	NP_001280141.1:p.Met287Val
NM_001293213.1:c.370-177A>G	NP_001280142.1:n.370-177A>G
NM_001293214.1:c.667A>G	NP_001280143.1:p.Met223Val
NM_001293215.1:c.583A>G	NP_001280144.1:p.Met195Val
NM_001293216.1:c.583A>G	NP_001280145.1:p.Met195Val
NM_178014.3:c.799A>G	NP_821133.1:p.Met267Val
NR_120608.1:n.584-78A>G
NM_178014.4:c.799A>G MANE Select	NP_821133.1:p.Met267Val
NM_001293212.2:c.859A>G	NP_001280141.1:p.Met287Val
NM_001293213.2:c.370-177A>G	NP_001280142.1:n.370-177A>G
NM_001293214.2:c.667A>G	NP_001280143.1:p.Met223Val
NM_001293215.2:c.583A>G	NP_001280144.1:p.Met195Val
NM_001293216.2:c.583A>G	NP_001280145.1:p.Met195Val
NR_120608.2:n.433-78A>G