Canonical Allele Identifier: CA363151713
Gene: TUBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30724303A>G , CM000668.2:g.30724303A>G GRCh38
NC_000006.11:g.30692080A>G , CM000668.1:g.30692080A>G GRCh37
NC_000006.10:g.30800059A>G NCBI36
NG_034142.1:g.9103A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.1241A>G MANE Select ENSP00000339001.7:p.Asn414Ser
ENST00000680530.1:n.2103A>G
ENST00000681421.1:n.2307A>G
ENST00000681435.1:c.1025A>G ENSP00000506665.1:p.Asn342Ser
ENST00000327892.12:c.1241A>G ENSP00000339001.7:p.Asn414Ser
ENST00000330914.7:c.1025A>G ENSP00000365578.2:p.Asn342Ser
ENST00000396384.1:c.1025A>G ENSP00000379668.1:p.Asn342Ser
ENST00000396389.5:c.1187A>G ENSP00000379672.1:p.Asn396Ser
NM_001293212.1:c.1301A>G NP_001280141.1:p.Asn434Ser
NM_001293213.1:c.635A>G NP_001280142.1:p.Asn212Ser
NM_001293214.1:c.1109A>G NP_001280143.1:p.Asn370Ser
NM_001293215.1:c.1025A>G NP_001280144.1:p.Asn342Ser
NM_001293216.1:c.1025A>G NP_001280145.1:p.Asn342Ser
NM_178014.3:c.1241A>G NP_821133.1:p.Asn414Ser
NR_120608.1:n.948A>G
NM_178014.4:c.1241A>G MANE Select NP_821133.1:p.Asn414Ser
NM_001293212.2:c.1301A>G NP_001280141.1:p.Asn434Ser
NM_001293213.2:c.635A>G NP_001280142.1:p.Asn212Ser
NM_001293214.2:c.1109A>G NP_001280143.1:p.Asn370Ser
NM_001293215.2:c.1025A>G NP_001280144.1:p.Asn342Ser
NM_001293216.2:c.1025A>G NP_001280145.1:p.Asn342Ser
NR_120608.2:n.797A>G