Canonical Allele Identifier: CA363141513

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30688336C>A (hg19) ; chr6:g.30720559C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30720559C>A , CM000668.2:g.30720559C>A	GRCh38
NC_000006.11:g.30688336C>A , CM000668.1:g.30688336C>A	GRCh37
NC_000006.10:g.30796315C>A	NCBI36
NG_034142.1:g.5359C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000327892.13:c.53C>A MANE Select	ENSP00000339001.7:p.Ala18Asp
ENST00000681435.1:c.-159-1978C>A	ENSP00000506665.1:n.-159-1978C>A
ENST00000327892.12:c.53C>A	ENSP00000339001.7:p.Ala18Asp
NM_001293213.1:c.53C>A	NP_001280142.1:p.Ala18Asp
NM_001293214.1:c.34+19C>A	NP_001280143.1:n.34+19C>A
NM_178014.3:c.53C>A	NP_821133.1:p.Ala18Asp
NR_120608.1:n.359C>A
NM_178014.4:c.53C>A MANE Select	NP_821133.1:p.Ala18Asp
NM_001293213.2:c.53C>A	NP_001280142.1:p.Ala18Asp
NM_001293214.2:c.34+19C>A	NP_001280143.1:n.34+19C>A
NR_120608.2:n.208C>A