Canonical Allele Identifier: CA379562591

Gene: TUB

Linked Data

• dbSNP Id: rs1372853481
• MyVariant Identifiers: chr11:g.8111631C>G (hg19) ; chr11:g.8090084C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090084C>G , CM000673.2:g.8090084C>G	GRCh38
NC_000011.9:g.8111631C>G , CM000673.1:g.8111631C>G	GRCh37
NC_000011.8:g.8068207C>G	NCBI36
NG_029912.1:g.56452C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.106C>G MANE Select	ENSP00000299506.3:p.Gln36Glu
ENST00000299506.2:c.106C>G	ENSP00000299506.2:p.Gln36Glu
ENST00000305253.8:c.271C>G	ENSP00000305426.4:p.Gln91Glu
ENST00000534099.5:c.124C>G	ENSP00000434400.1:p.Gln42Glu
NM_003320.4:c.271C>G	NP_003311.2:p.Gln91Glu
NM_177972.2:c.106C>G	NP_813977.1:p.Gln36Glu
XM_005253109.2:c.232C>G	XP_005253166.1:p.Gln78Glu
XM_011520344.1:c.142C>G	XP_011518646.1:p.Gln48Glu
XM_005253109.3:c.232C>G	XP_005253166.1:p.Gln78Glu
XM_011520344.2:c.142C>G	XP_011518646.1:p.Gln48Glu
NM_177972.3:c.106C>G MANE Select	NP_813977.1:p.Gln36Glu
NM_003320.5:c.271C>G	NP_003311.2:p.Gln91Glu