Canonical Allele Identifier: CA363151632

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30692064A>T (hg19) ; chr6:g.30724287A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724287A>T , CM000668.2:g.30724287A>T	GRCh38
NC_000006.11:g.30692064A>T , CM000668.1:g.30692064A>T	GRCh37
NC_000006.10:g.30800043A>T	NCBI36
NG_034142.1:g.9087A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1225A>T MANE Select	ENSP00000339001.7:p.Thr409Ser
ENST00000680530.1:n.2087A>T
ENST00000681421.1:n.2291A>T
ENST00000681435.1:c.1009A>T	ENSP00000506665.1:p.Thr337Ser
ENST00000327892.12:c.1225A>T	ENSP00000339001.7:p.Thr409Ser
ENST00000330914.7:c.1009A>T	ENSP00000365578.2:p.Thr337Ser
ENST00000396384.1:c.1009A>T	ENSP00000379668.1:p.Thr337Ser
ENST00000396389.5:c.1171A>T	ENSP00000379672.1:p.Thr391Ser
NM_001293212.1:c.1285A>T	NP_001280141.1:p.Thr429Ser
NM_001293213.1:c.619A>T	NP_001280142.1:p.Thr207Ser
NM_001293214.1:c.1093A>T	NP_001280143.1:p.Thr365Ser
NM_001293215.1:c.1009A>T	NP_001280144.1:p.Thr337Ser
NM_001293216.1:c.1009A>T	NP_001280145.1:p.Thr337Ser
NM_178014.3:c.1225A>T	NP_821133.1:p.Thr409Ser
NR_120608.1:n.932A>T
NM_178014.4:c.1225A>T MANE Select	NP_821133.1:p.Thr409Ser
NM_001293212.2:c.1285A>T	NP_001280141.1:p.Thr429Ser
NM_001293213.2:c.619A>T	NP_001280142.1:p.Thr207Ser
NM_001293214.2:c.1093A>T	NP_001280143.1:p.Thr365Ser
NM_001293215.2:c.1009A>T	NP_001280144.1:p.Thr337Ser
NM_001293216.2:c.1009A>T	NP_001280145.1:p.Thr337Ser
NR_120608.2:n.781A>T