Canonical Allele Identifier: CA449776609

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691625T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723848T>A , CM000668.2:g.30723848T>A	GRCh38
NC_000006.11:g.30691625T>A , CM000668.1:g.30691625T>A	GRCh37
NC_000006.10:g.30799604T>A	NCBI36
NG_034142.1:g.8648T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.786T>A MANE Select	ENSP00000339001.7:p.Arg262=
ENST00000680530.1:n.1648T>A
ENST00000681421.1:n.1852T>A
ENST00000681435.1:c.570T>A	ENSP00000506665.1:p.Arg190=
ENST00000327892.12:c.786T>A	ENSP00000339001.7:p.Arg262=
ENST00000330914.7:c.570T>A	ENSP00000365578.2:p.Arg190=
ENST00000396384.1:c.570T>A	ENSP00000379668.1:p.Arg190=
ENST00000396389.5:c.732T>A	ENSP00000379672.1:p.Arg244=
NM_001293212.1:c.846T>A	NP_001280141.1:p.Arg282=
NM_001293213.1:c.370-190T>A	NP_001280142.1:n.370-190T>A
NM_001293214.1:c.654T>A	NP_001280143.1:p.Arg218=
NM_001293215.1:c.570T>A	NP_001280144.1:p.Arg190=
NM_001293216.1:c.570T>A	NP_001280145.1:p.Arg190=
NM_178014.3:c.786T>A	NP_821133.1:p.Arg262=
NR_120608.1:n.584-91T>A
NM_178014.4:c.786T>A MANE Select	NP_821133.1:p.Arg262=
NM_001293212.2:c.846T>A	NP_001280141.1:p.Arg282=
NM_001293213.2:c.370-190T>A	NP_001280142.1:n.370-190T>A
NM_001293214.2:c.654T>A	NP_001280143.1:p.Arg218=
NM_001293215.2:c.570T>A	NP_001280144.1:p.Arg190=
NM_001293216.2:c.570T>A	NP_001280145.1:p.Arg190=
NR_120608.2:n.433-91T>A