Canonical Allele Identifier: CA449776564

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691604C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723827C>A , CM000668.2:g.30723827C>A	GRCh38
NC_000006.11:g.30691604C>A , CM000668.1:g.30691604C>A	GRCh37
NC_000006.10:g.30799583C>A	NCBI36
NG_034142.1:g.8627C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.765C>A MANE Select	ENSP00000339001.7:p.Val255=
ENST00000680530.1:n.1627C>A
ENST00000681421.1:n.1831C>A
ENST00000681435.1:c.549C>A	ENSP00000506665.1:p.Val183=
ENST00000327892.12:c.765C>A	ENSP00000339001.7:p.Val255=
ENST00000330914.7:c.549C>A	ENSP00000365578.2:p.Val183=
ENST00000396384.1:c.549C>A	ENSP00000379668.1:p.Val183=
ENST00000396389.5:c.711C>A	ENSP00000379672.1:p.Val237=
NM_001293212.1:c.825C>A	NP_001280141.1:p.Val275=
NM_001293213.1:c.370-211C>A	NP_001280142.1:n.370-211C>A
NM_001293214.1:c.633C>A	NP_001280143.1:p.Val211=
NM_001293215.1:c.549C>A	NP_001280144.1:p.Val183=
NM_001293216.1:c.549C>A	NP_001280145.1:p.Val183=
NM_178014.3:c.765C>A	NP_821133.1:p.Val255=
NR_120608.1:n.584-112C>A
NM_178014.4:c.765C>A MANE Select	NP_821133.1:p.Val255=
NM_001293212.2:c.825C>A	NP_001280141.1:p.Val275=
NM_001293213.2:c.370-211C>A	NP_001280142.1:n.370-211C>A
NM_001293214.2:c.633C>A	NP_001280143.1:p.Val211=
NM_001293215.2:c.549C>A	NP_001280144.1:p.Val183=
NM_001293216.2:c.549C>A	NP_001280145.1:p.Val183=
NR_120608.2:n.433-112C>A