Canonical Allele Identifier: CA680747440

Gene: TUB

Linked Data

• dbSNP Id: rs1346225948
• gnomAD v3: 11-8090138-GGGCGGCCCCGGAGCC-G
• gnomAD v4: 11-8090138-GGGCGGCCCCGGAGCC-G
• MyVariant Identifiers: chr11:g.8111686_8111700del (hg19) ; chr11:g.8090139_8090153del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090144_8090158del , CM000673.2:g.8090144_8090158del	GRCh38
NC_000011.9:g.8111691_8111705del , CM000673.1:g.8111691_8111705del	GRCh37
NC_000011.8:g.8068267_8068281del	NCBI36
NG_029912.1:g.56512_56526del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.166_180del MANE Select	ENSP00000299506.3:p.Pro56_Arg60del
ENST00000299506.2:c.166_180del	ENSP00000299506.2:p.Pro56_Arg60del
ENST00000305253.8:c.331_345del	ENSP00000305426.4:p.Pro111_Arg115del
ENST00000534099.5:c.184_198del	ENSP00000434400.1:p.Pro62_Arg66del
NM_003320.4:c.331_345del	NP_003311.2:p.Pro111_Arg115del
NM_177972.2:c.166_180del	NP_813977.1:p.Pro56_Arg60del
XM_005253109.2:c.292_306del	XP_005253166.1:p.Pro98_Arg102del
XM_011520344.1:c.202_216del	XP_011518646.1:p.Pro68_Arg72del
XM_005253109.3:c.292_306del	XP_005253166.1:p.Pro98_Arg102del
XM_011520344.2:c.202_216del	XP_011518646.1:p.Pro68_Arg72del
NM_177972.3:c.166_180del MANE Select	NP_813977.1:p.Pro56_Arg60del
NM_003320.5:c.331_345del	NP_003311.2:p.Pro111_Arg115del