Canonical Allele Identifier: CA379562999

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111727G>T (hg19) ; chr11:g.8090180G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090180G>T , CM000673.2:g.8090180G>T	GRCh38
NC_000011.9:g.8111727G>T , CM000673.1:g.8111727G>T	GRCh37
NC_000011.8:g.8068303G>T	NCBI36
NG_029912.1:g.56548G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.202G>T MANE Select	ENSP00000299506.3:p.Ala68Ser
ENST00000299506.2:c.202G>T	ENSP00000299506.2:p.Ala68Ser
ENST00000305253.8:c.367G>T	ENSP00000305426.4:p.Ala123Ser
ENST00000534099.5:c.220G>T	ENSP00000434400.1:p.Ala74Ser
NM_003320.4:c.367G>T	NP_003311.2:p.Ala123Ser
NM_177972.2:c.202G>T	NP_813977.1:p.Ala68Ser
XM_005253109.2:c.328G>T	XP_005253166.1:p.Ala110Ser
XM_011520344.1:c.238G>T	XP_011518646.1:p.Ala80Ser
XM_005253109.3:c.328G>T	XP_005253166.1:p.Ala110Ser
XM_011520344.2:c.238G>T	XP_011518646.1:p.Ala80Ser
NM_177972.3:c.202G>T MANE Select	NP_813977.1:p.Ala68Ser
NM_003320.5:c.367G>T	NP_003311.2:p.Ala123Ser