Canonical Allele Identifier: CA379562796

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111679G>T (hg19) ; chr11:g.8090132G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090132G>T , CM000673.2:g.8090132G>T	GRCh38
NC_000011.9:g.8111679G>T , CM000673.1:g.8111679G>T	GRCh37
NC_000011.8:g.8068255G>T	NCBI36
NG_029912.1:g.56500G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.154G>T MANE Select	ENSP00000299506.3:p.Ala52Ser
ENST00000299506.2:c.154G>T	ENSP00000299506.2:p.Ala52Ser
ENST00000305253.8:c.319G>T	ENSP00000305426.4:p.Ala107Ser
ENST00000534099.5:c.172G>T	ENSP00000434400.1:p.Ala58Ser
NM_003320.4:c.319G>T	NP_003311.2:p.Ala107Ser
NM_177972.2:c.154G>T	NP_813977.1:p.Ala52Ser
XM_005253109.2:c.280G>T	XP_005253166.1:p.Ala94Ser
XM_011520344.1:c.190G>T	XP_011518646.1:p.Ala64Ser
XM_005253109.3:c.280G>T	XP_005253166.1:p.Ala94Ser
XM_011520344.2:c.190G>T	XP_011518646.1:p.Ala64Ser
NM_177972.3:c.154G>T MANE Select	NP_813977.1:p.Ala52Ser
NM_003320.5:c.319G>T	NP_003311.2:p.Ala107Ser