Canonical Allele Identifier: CA5870955

Gene: TUB

Linked Data

• dbSNP Id: rs751242481
• ExAC: 11:8111599 CCT / C
• gnomAD v2: 11-8111599-CCT-C
• gnomAD v4: 11-8090052-CCT-C
• MyVariant Identifiers: chr11:g.8111600_8111601del (hg19) ; chr11:g.8090053_8090054del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090055_8090056del , CM000673.2:g.8090055_8090056del	GRCh38
NC_000011.9:g.8111602_8111603del , CM000673.1:g.8111602_8111603del	GRCh37
NC_000011.8:g.8068178_8068179del	NCBI36
NG_029912.1:g.56423_56424del

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.91-14_91-13del MANE Select	ENSP00000299506.3:n.91-14_91-13del
ENST00000299506.2:c.91-14_91-13del	ENSP00000299506.2:n.91-14_91-13del
ENST00000305253.8:c.256-14_256-13del	ENSP00000305426.4:n.256-14_256-13del
ENST00000534099.5:c.109-14_109-13del	ENSP00000434400.1:n.109-14_109-13del
NM_003320.4:c.256-14_256-13del	NP_003311.2:n.256-14_256-13del
NM_177972.2:c.91-14_91-13del	NP_813977.1:n.91-14_91-13del
XM_005253109.2:c.217-14_217-13del	XP_005253166.1:n.217-14_217-13del
XM_011520344.1:c.127-14_127-13del	XP_011518646.1:n.127-14_127-13del
XM_005253109.3:c.217-14_217-13del	XP_005253166.1:n.217-14_217-13del
XM_011520344.2:c.127-14_127-13del	XP_011518646.1:n.127-14_127-13del
NM_177972.3:c.91-14_91-13del MANE Select	NP_813977.1:n.91-14_91-13del
NM_003320.5:c.256-14_256-13del	NP_003311.2:n.256-14_256-13del