Canonical Allele Identifier: CA379563231

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111778G>T (hg19) ; chr11:g.8090231G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090231G>T , CM000673.2:g.8090231G>T	GRCh38
NC_000011.9:g.8111778G>T , CM000673.1:g.8111778G>T	GRCh37
NC_000011.8:g.8068354G>T	NCBI36
NG_029912.1:g.56599G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.253G>T MANE Select	ENSP00000299506.3:p.Val85Phe
ENST00000299506.2:c.253G>T	ENSP00000299506.2:p.Val85Phe
ENST00000305253.8:c.418G>T	ENSP00000305426.4:p.Val140Phe
ENST00000534099.5:c.271G>T	ENSP00000434400.1:p.Val91Phe
NM_003320.4:c.418G>T	NP_003311.2:p.Val140Phe
NM_177972.2:c.253G>T	NP_813977.1:p.Val85Phe
XM_005253109.2:c.379G>T	XP_005253166.1:p.Val127Phe
XM_011520344.1:c.289G>T	XP_011518646.1:p.Val97Phe
XM_005253109.3:c.379G>T	XP_005253166.1:p.Val127Phe
XM_011520344.2:c.289G>T	XP_011518646.1:p.Val97Phe
NM_177972.3:c.253G>T MANE Select	NP_813977.1:p.Val85Phe
NM_003320.5:c.418G>T	NP_003311.2:p.Val140Phe