Canonical Allele Identifier: CA363148547
Gene: TUBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30723835T>G , CM000668.2:g.30723835T>G GRCh38
NC_000006.11:g.30691612T>G , CM000668.1:g.30691612T>G GRCh37
NC_000006.10:g.30799591T>G NCBI36
NG_034142.1:g.8635T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.773T>G MANE Select ENSP00000339001.7:p.Val258Gly
ENST00000680530.1:n.1635T>G
ENST00000681421.1:n.1839T>G
ENST00000681435.1:c.557T>G ENSP00000506665.1:p.Val186Gly
ENST00000327892.12:c.773T>G ENSP00000339001.7:p.Val258Gly
ENST00000330914.7:c.557T>G ENSP00000365578.2:p.Val186Gly
ENST00000396384.1:c.557T>G ENSP00000379668.1:p.Val186Gly
ENST00000396389.5:c.719T>G ENSP00000379672.1:p.Val240Gly
NM_001293212.1:c.833T>G NP_001280141.1:p.Val278Gly
NM_001293213.1:c.370-203T>G NP_001280142.1:n.370-203T>G
NM_001293214.1:c.641T>G NP_001280143.1:p.Val214Gly
NM_001293215.1:c.557T>G NP_001280144.1:p.Val186Gly
NM_001293216.1:c.557T>G NP_001280145.1:p.Val186Gly
NM_178014.3:c.773T>G NP_821133.1:p.Val258Gly
NR_120608.1:n.584-104T>G
NM_178014.4:c.773T>G MANE Select NP_821133.1:p.Val258Gly
NM_001293212.2:c.833T>G NP_001280141.1:p.Val278Gly
NM_001293213.2:c.370-203T>G NP_001280142.1:n.370-203T>G
NM_001293214.2:c.641T>G NP_001280143.1:p.Val214Gly
NM_001293215.2:c.557T>G NP_001280144.1:p.Val186Gly
NM_001293216.2:c.557T>G NP_001280145.1:p.Val186Gly
NR_120608.2:n.433-104T>G