Canonical Allele Identifier: CA363149075
Gene: TUBB HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.898A>T MANE Select ENSP00000339001.7:p.Met300Leu
ENST00000680530.1:n.1760A>T
ENST00000681421.1:n.1964A>T
ENST00000681435.1:c.682A>T ENSP00000506665.1:p.Met228Leu
ENST00000327892.12:c.898A>T ENSP00000339001.7:p.Met300Leu
ENST00000330914.7:c.682A>T ENSP00000365578.2:p.Met228Leu
ENST00000396384.1:c.682A>T ENSP00000379668.1:p.Met228Leu
ENST00000396389.5:c.844A>T ENSP00000379672.1:p.Met282Leu
NM_001293212.1:c.958A>T NP_001280141.1:p.Met320Leu
NM_001293213.1:c.370-78A>T NP_001280142.1:n.370-78A>T
NM_001293214.1:c.766A>T NP_001280143.1:p.Met256Leu
NM_001293215.1:c.682A>T NP_001280144.1:p.Met228Leu
NM_001293216.1:c.682A>T NP_001280145.1:p.Met228Leu
NM_178014.3:c.898A>T NP_821133.1:p.Met300Leu
NR_120608.1:n.605A>T
NM_178014.4:c.898A>T MANE Select NP_821133.1:p.Met300Leu
NM_001293212.2:c.958A>T NP_001280141.1:p.Met320Leu
NM_001293213.2:c.370-78A>T NP_001280142.1:n.370-78A>T
NM_001293214.2:c.766A>T NP_001280143.1:p.Met256Leu
NM_001293215.2:c.682A>T NP_001280144.1:p.Met228Leu
NM_001293216.2:c.682A>T NP_001280145.1:p.Met228Leu
NR_120608.2:n.454A>T