Canonical Allele Identifier: CA379562239

Gene: TUB

Linked Data

• gnomAD v4: 11-8089611-G-T
• MyVariant Identifiers: chr11:g.8111158G>T (hg19) ; chr11:g.8089611G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089611G>T , CM000673.2:g.8089611G>T	GRCh38
NC_000011.9:g.8111158G>T , CM000673.1:g.8111158G>T	GRCh37
NC_000011.8:g.8067734G>T	NCBI36
NG_029912.1:g.55979G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.40G>T MANE Select	ENSP00000299506.3:p.Val14Phe
ENST00000299506.2:c.40G>T	ENSP00000299506.2:p.Val14Phe
ENST00000305253.8:c.205G>T	ENSP00000305426.4:p.Val69Phe
ENST00000534099.5:c.58G>T	ENSP00000434400.1:p.Val20Phe
NM_003320.4:c.205G>T	NP_003311.2:p.Val69Phe
NM_177972.2:c.40G>T	NP_813977.1:p.Val14Phe
XM_005253109.2:c.166G>T	XP_005253166.1:p.Val56Phe
XM_011520344.1:c.76G>T	XP_011518646.1:p.Val26Phe
XM_005253109.3:c.166G>T	XP_005253166.1:p.Val56Phe
XM_011520344.2:c.76G>T	XP_011518646.1:p.Val26Phe
NM_177972.3:c.40G>T MANE Select	NP_813977.1:p.Val14Phe
NM_003320.5:c.205G>T	NP_003311.2:p.Val69Phe