Canonical Allele Identifier: CA379562555

Gene: TUB

Linked Data

• gnomAD v4: 11-8090075-C-A
• MyVariant Identifiers: chr11:g.8111622C>A (hg19) ; chr11:g.8090075C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090075C>A , CM000673.2:g.8090075C>A	GRCh38
NC_000011.9:g.8111622C>A , CM000673.1:g.8111622C>A	GRCh37
NC_000011.8:g.8068198C>A	NCBI36
NG_029912.1:g.56443C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.97C>A MANE Select	ENSP00000299506.3:p.Leu33Met
ENST00000299506.2:c.97C>A	ENSP00000299506.2:p.Leu33Met
ENST00000305253.8:c.262C>A	ENSP00000305426.4:p.Leu88Met
ENST00000534099.5:c.115C>A	ENSP00000434400.1:p.Leu39Met
NM_003320.4:c.262C>A	NP_003311.2:p.Leu88Met
NM_177972.2:c.97C>A	NP_813977.1:p.Leu33Met
XM_005253109.2:c.223C>A	XP_005253166.1:p.Leu75Met
XM_011520344.1:c.133C>A	XP_011518646.1:p.Leu45Met
XM_005253109.3:c.223C>A	XP_005253166.1:p.Leu75Met
XM_011520344.2:c.133C>A	XP_011518646.1:p.Leu45Met
NM_177972.3:c.97C>A MANE Select	NP_813977.1:p.Leu33Met
NM_003320.5:c.262C>A	NP_003311.2:p.Leu88Met