Canonical Allele Identifier: CA449777125

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30692009C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724232C>T , CM000668.2:g.30724232C>T	GRCh38
NC_000006.11:g.30692009C>T , CM000668.1:g.30692009C>T	GRCh37
NC_000006.10:g.30799988C>T	NCBI36
NG_034142.1:g.9032C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1170C>T MANE Select	ENSP00000339001.7:p.Arg390=
ENST00000680530.1:n.2032C>T
ENST00000681421.1:n.2236C>T
ENST00000681435.1:c.954C>T	ENSP00000506665.1:p.Arg318=
ENST00000327892.12:c.1170C>T	ENSP00000339001.7:p.Arg390=
ENST00000330914.7:c.954C>T	ENSP00000365578.2:p.Arg318=
ENST00000396384.1:c.954C>T	ENSP00000379668.1:p.Arg318=
ENST00000396389.5:c.1116C>T	ENSP00000379672.1:p.Arg372=
NM_001293212.1:c.1230C>T	NP_001280141.1:p.Arg410=
NM_001293213.1:c.564C>T	NP_001280142.1:p.Arg188=
NM_001293214.1:c.1038C>T	NP_001280143.1:p.Arg346=
NM_001293215.1:c.954C>T	NP_001280144.1:p.Arg318=
NM_001293216.1:c.954C>T	NP_001280145.1:p.Arg318=
NM_178014.3:c.1170C>T	NP_821133.1:p.Arg390=
NR_120608.1:n.877C>T
NM_178014.4:c.1170C>T MANE Select	NP_821133.1:p.Arg390=
NM_001293212.2:c.1230C>T	NP_001280141.1:p.Arg410=
NM_001293213.2:c.564C>T	NP_001280142.1:p.Arg188=
NM_001293214.2:c.1038C>T	NP_001280143.1:p.Arg346=
NM_001293215.2:c.954C>T	NP_001280144.1:p.Arg318=
NM_001293216.2:c.954C>T	NP_001280145.1:p.Arg318=
NR_120608.2:n.726C>T