Canonical Allele Identifier: CA363150508

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691906T>A (hg19) ; chr6:g.30724129T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724129T>A , CM000668.2:g.30724129T>A	GRCh38
NC_000006.11:g.30691906T>A , CM000668.1:g.30691906T>A	GRCh37
NC_000006.10:g.30799885T>A	NCBI36
NG_034142.1:g.8929T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1067T>A MANE Select	ENSP00000339001.7:p.Ile356Asn
ENST00000680530.1:n.1929T>A
ENST00000681421.1:n.2133T>A
ENST00000681435.1:c.851T>A	ENSP00000506665.1:p.Ile284Asn
ENST00000327892.12:c.1067T>A	ENSP00000339001.7:p.Ile356Asn
ENST00000330914.7:c.851T>A	ENSP00000365578.2:p.Ile284Asn
ENST00000396384.1:c.851T>A	ENSP00000379668.1:p.Ile284Asn
ENST00000396389.5:c.1013T>A	ENSP00000379672.1:p.Ile338Asn
NM_001293212.1:c.1127T>A	NP_001280141.1:p.Ile376Asn
NM_001293213.1:c.461T>A	NP_001280142.1:p.Ile154Asn
NM_001293214.1:c.935T>A	NP_001280143.1:p.Ile312Asn
NM_001293215.1:c.851T>A	NP_001280144.1:p.Ile284Asn
NM_001293216.1:c.851T>A	NP_001280145.1:p.Ile284Asn
NM_178014.3:c.1067T>A	NP_821133.1:p.Ile356Asn
NR_120608.1:n.774T>A
NM_178014.4:c.1067T>A MANE Select	NP_821133.1:p.Ile356Asn
NM_001293212.2:c.1127T>A	NP_001280141.1:p.Ile376Asn
NM_001293213.2:c.461T>A	NP_001280142.1:p.Ile154Asn
NM_001293214.2:c.935T>A	NP_001280143.1:p.Ile312Asn
NM_001293215.2:c.851T>A	NP_001280144.1:p.Ile284Asn
NM_001293216.2:c.851T>A	NP_001280145.1:p.Ile284Asn
NR_120608.2:n.623T>A