Canonical Allele Identifier: CA379563238

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111779G>T (hg19) ; chr11:g.8090232G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090232G>T , CM000673.2:g.8090232G>T	GRCh38
NC_000011.9:g.8111779G>T , CM000673.1:g.8111779G>T	GRCh37
NC_000011.8:g.8068355G>T	NCBI36
NG_029912.1:g.56600G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.253+1G>T MANE Select	ENSP00000299506.3:n.253+1G>T
ENST00000299506.2:c.253+1G>T	ENSP00000299506.2:n.253+1G>T
ENST00000305253.8:c.418+1G>T	ENSP00000305426.4:n.418+1G>T
ENST00000534099.5:c.271+1G>T	ENSP00000434400.1:n.271+1G>T
NM_003320.4:c.418+1G>T	NP_003311.2:n.418+1G>T
NM_177972.2:c.253+1G>T	NP_813977.1:n.253+1G>T
XM_005253109.2:c.379+1G>T	XP_005253166.1:n.379+1G>T
XM_011520344.1:c.289+1G>T	XP_011518646.1:n.289+1G>T
XM_005253109.3:c.379+1G>T	XP_005253166.1:n.379+1G>T
XM_011520344.2:c.289+1G>T	XP_011518646.1:n.289+1G>T
NM_177972.3:c.253+1G>T MANE Select	NP_813977.1:n.253+1G>T
NM_003320.5:c.418+1G>T	NP_003311.2:n.418+1G>T