Canonical Allele Identifier: CA379562676

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111652C>A (hg19) ; chr11:g.8090105C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090105C>A , CM000673.2:g.8090105C>A	GRCh38
NC_000011.9:g.8111652C>A , CM000673.1:g.8111652C>A	GRCh37
NC_000011.8:g.8068228C>A	NCBI36
NG_029912.1:g.56473C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.127C>A MANE Select	ENSP00000299506.3:p.Gln43Lys
ENST00000299506.2:c.127C>A	ENSP00000299506.2:p.Gln43Lys
ENST00000305253.8:c.292C>A	ENSP00000305426.4:p.Gln98Lys
ENST00000534099.5:c.145C>A	ENSP00000434400.1:p.Gln49Lys
NM_003320.4:c.292C>A	NP_003311.2:p.Gln98Lys
NM_177972.2:c.127C>A	NP_813977.1:p.Gln43Lys
XM_005253109.2:c.253C>A	XP_005253166.1:p.Gln85Lys
XM_011520344.1:c.163C>A	XP_011518646.1:p.Gln55Lys
XM_005253109.3:c.253C>A	XP_005253166.1:p.Gln85Lys
XM_011520344.2:c.163C>A	XP_011518646.1:p.Gln55Lys
NM_177972.3:c.127C>A MANE Select	NP_813977.1:p.Gln43Lys
NM_003320.5:c.292C>A	NP_003311.2:p.Gln98Lys