Canonical Allele Identifier: CA1950952570

Gene: TUB

Linked Data

• dbSNP Id: rs1943730249
• gnomAD v4: 11-8089483-GCTCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089486_8089489del , CM000673.2:g.8089486_8089489del	GRCh38
NC_000011.9:g.8111033_8111036del , CM000673.1:g.8111033_8111036del	GRCh37
NC_000011.8:g.8067609_8067612del	NCBI36
NG_029912.1:g.55854_55857del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39-124_39-121del MANE Select	ENSP00000299506.3:n.39-124_39-121del
ENST00000299506.2:c.39-124_39-121del	ENSP00000299506.2:n.39-124_39-121del
ENST00000305253.8:c.204-124_204-121del	ENSP00000305426.4:n.204-124_204-121del
ENST00000534099.5:c.57-124_57-121del	ENSP00000434400.1:n.57-124_57-121del
NM_003320.4:c.204-124_204-121del	NP_003311.2:n.204-124_204-121del
NM_177972.2:c.39-124_39-121del	NP_813977.1:n.39-124_39-121del
XM_005253109.2:c.165-124_165-121del	XP_005253166.1:n.165-124_165-121del
XM_011520344.1:c.75-124_75-121del	XP_011518646.1:n.75-124_75-121del
XM_005253109.3:c.165-124_165-121del	XP_005253166.1:n.165-124_165-121del
XM_011520344.2:c.75-124_75-121del	XP_011518646.1:n.75-124_75-121del
NM_177972.3:c.39-124_39-121del MANE Select	NP_813977.1:n.39-124_39-121del
NM_003320.5:c.204-124_204-121del	NP_003311.2:n.204-124_204-121del