Canonical Allele Identifier: CA379562801

Gene: TUB

Linked Data

• dbSNP Id: rs1197544129
• gnomAD v2: 11-8111680-C-T
• gnomAD v4: 11-8090133-C-T
• MyVariant Identifiers: chr11:g.8111680C>T (hg19) ; chr11:g.8090133C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090133C>T , CM000673.2:g.8090133C>T	GRCh38
NC_000011.9:g.8111680C>T , CM000673.1:g.8111680C>T	GRCh37
NC_000011.8:g.8068256C>T	NCBI36
NG_029912.1:g.56501C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.155C>T MANE Select	ENSP00000299506.3:p.Ala52Val
ENST00000299506.2:c.155C>T	ENSP00000299506.2:p.Ala52Val
ENST00000305253.8:c.320C>T	ENSP00000305426.4:p.Ala107Val
ENST00000534099.5:c.173C>T	ENSP00000434400.1:p.Ala58Val
NM_003320.4:c.320C>T	NP_003311.2:p.Ala107Val
NM_177972.2:c.155C>T	NP_813977.1:p.Ala52Val
XM_005253109.2:c.281C>T	XP_005253166.1:p.Ala94Val
XM_011520344.1:c.191C>T	XP_011518646.1:p.Ala64Val
XM_005253109.3:c.281C>T	XP_005253166.1:p.Ala94Val
XM_011520344.2:c.191C>T	XP_011518646.1:p.Ala64Val
NM_177972.3:c.155C>T MANE Select	NP_813977.1:p.Ala52Val
NM_003320.5:c.320C>T	NP_003311.2:p.Ala107Val