Canonical Allele Identifier: CA363149362
Gene: TUBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30723999G>C , CM000668.2:g.30723999G>C GRCh38
NC_000006.11:g.30691776G>C , CM000668.1:g.30691776G>C GRCh37
NC_000006.10:g.30799755G>C NCBI36
NG_034142.1:g.8799G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.937G>C MANE Select ENSP00000339001.7:p.Val313Leu
ENST00000680530.1:n.1799G>C
ENST00000681421.1:n.2003G>C
ENST00000681435.1:c.721G>C ENSP00000506665.1:p.Val241Leu
ENST00000327892.12:c.937G>C ENSP00000339001.7:p.Val313Leu
ENST00000330914.7:c.721G>C ENSP00000365578.2:p.Val241Leu
ENST00000396384.1:c.721G>C ENSP00000379668.1:p.Val241Leu
ENST00000396389.5:c.883G>C ENSP00000379672.1:p.Val295Leu
NM_001293212.1:c.997G>C NP_001280141.1:p.Val333Leu
NM_001293213.1:c.370-39G>C NP_001280142.1:n.370-39G>C
NM_001293214.1:c.805G>C NP_001280143.1:p.Val269Leu
NM_001293215.1:c.721G>C NP_001280144.1:p.Val241Leu
NM_001293216.1:c.721G>C NP_001280145.1:p.Val241Leu
NM_178014.3:c.937G>C NP_821133.1:p.Val313Leu
NR_120608.1:n.644G>C
NM_178014.4:c.937G>C MANE Select NP_821133.1:p.Val313Leu
NM_001293212.2:c.997G>C NP_001280141.1:p.Val333Leu
NM_001293213.2:c.370-39G>C NP_001280142.1:n.370-39G>C
NM_001293214.2:c.805G>C NP_001280143.1:p.Val269Leu
NM_001293215.2:c.721G>C NP_001280144.1:p.Val241Leu
NM_001293216.2:c.721G>C NP_001280145.1:p.Val241Leu
NR_120608.2:n.493G>C