Canonical Allele Identifier: CA449776898

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691797C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724020C>A , CM000668.2:g.30724020C>A	GRCh38
NC_000006.11:g.30691797C>A , CM000668.1:g.30691797C>A	GRCh37
NC_000006.10:g.30799776C>A	NCBI36
NG_034142.1:g.8820C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000327892.13:c.958C>A MANE Select	ENSP00000339001.7:p.Arg320=
ENST00000680530.1:n.1820C>A
ENST00000681421.1:n.2024C>A
ENST00000681435.1:c.742C>A	ENSP00000506665.1:p.Arg248=
ENST00000327892.12:c.958C>A	ENSP00000339001.7:p.Arg320=
ENST00000330914.7:c.742C>A	ENSP00000365578.2:p.Arg248=
ENST00000396384.1:c.742C>A	ENSP00000379668.1:p.Arg248=
ENST00000396389.5:c.904C>A	ENSP00000379672.1:p.Arg302=
NM_001293212.1:c.1018C>A	NP_001280141.1:p.Arg340=
NM_001293213.1:c.370-18C>A	NP_001280142.1:n.370-18C>A
NM_001293214.1:c.826C>A	NP_001280143.1:p.Arg276=
NM_001293215.1:c.742C>A	NP_001280144.1:p.Arg248=
NM_001293216.1:c.742C>A	NP_001280145.1:p.Arg248=
NM_178014.3:c.958C>A	NP_821133.1:p.Arg320=
NR_120608.1:n.665C>A
NM_178014.4:c.958C>A MANE Select	NP_821133.1:p.Arg320=
NM_001293212.2:c.1018C>A	NP_001280141.1:p.Arg340=
NM_001293213.2:c.370-18C>A	NP_001280142.1:n.370-18C>A
NM_001293214.2:c.826C>A	NP_001280143.1:p.Arg276=
NM_001293215.2:c.742C>A	NP_001280144.1:p.Arg248=
NM_001293216.2:c.742C>A	NP_001280145.1:p.Arg248=
NR_120608.2:n.514C>A