Canonical Allele Identifier: CA379562596

Gene: TUB

Linked Data

• gnomAD v4: 11-8090085-A-G
• MyVariant Identifiers: chr11:g.8111632A>G (hg19) ; chr11:g.8090085A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090085A>G , CM000673.2:g.8090085A>G	GRCh38
NC_000011.9:g.8111632A>G , CM000673.1:g.8111632A>G	GRCh37
NC_000011.8:g.8068208A>G	NCBI36
NG_029912.1:g.56453A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.107A>G MANE Select	ENSP00000299506.3:p.Gln36Arg
ENST00000299506.2:c.107A>G	ENSP00000299506.2:p.Gln36Arg
ENST00000305253.8:c.272A>G	ENSP00000305426.4:p.Gln91Arg
ENST00000534099.5:c.125A>G	ENSP00000434400.1:p.Gln42Arg
NM_003320.4:c.272A>G	NP_003311.2:p.Gln91Arg
NM_177972.2:c.107A>G	NP_813977.1:p.Gln36Arg
XM_005253109.2:c.233A>G	XP_005253166.1:p.Gln78Arg
XM_011520344.1:c.143A>G	XP_011518646.1:p.Gln48Arg
XM_005253109.3:c.233A>G	XP_005253166.1:p.Gln78Arg
XM_011520344.2:c.143A>G	XP_011518646.1:p.Gln48Arg
NM_177972.3:c.107A>G MANE Select	NP_813977.1:p.Gln36Arg
NM_003320.5:c.272A>G	NP_003311.2:p.Gln91Arg