Canonical Allele Identifier: CA5870951

Gene: TUB

Linked Data

• dbSNP Id: rs749614540
• ExAC: 11:8111574 C / T
• gnomAD v4: 11-8090027-C-T
• MyVariant Identifiers: chr11:g.8111574C>T (hg19) ; chr11:g.8090027C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090027C>T , CM000673.2:g.8090027C>T	GRCh38
NC_000011.9:g.8111574C>T , CM000673.1:g.8111574C>T	GRCh37
NC_000011.8:g.8068150C>T	NCBI36
NG_029912.1:g.56395C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.91-42C>T MANE Select	ENSP00000299506.3:n.91-42C>T
ENST00000299506.2:c.91-42C>T	ENSP00000299506.2:n.91-42C>T
ENST00000305253.8:c.256-42C>T	ENSP00000305426.4:n.256-42C>T
ENST00000534099.5:c.109-42C>T	ENSP00000434400.1:n.109-42C>T
NM_003320.4:c.256-42C>T	NP_003311.2:n.256-42C>T
NM_177972.2:c.91-42C>T	NP_813977.1:n.91-42C>T
XM_005253109.2:c.217-42C>T	XP_005253166.1:n.217-42C>T
XM_011520344.1:c.127-42C>T	XP_011518646.1:n.127-42C>T
XM_005253109.3:c.217-42C>T	XP_005253166.1:n.217-42C>T
XM_011520344.2:c.127-42C>T	XP_011518646.1:n.127-42C>T
NM_177972.3:c.91-42C>T MANE Select	NP_813977.1:n.91-42C>T
NM_003320.5:c.256-42C>T	NP_003311.2:n.256-42C>T