Canonical Allele Identifier: CA1950953402

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090138_8090153delinsGGGCGGCCCCGGAGCC , CM000673.2:g.8090138_8090153delinsGGGCGGCCCCGGAGCC	GRCh38
NC_000011.9:g.8111685_8111700delinsGGGCGGCCCCGGAGCC , CM000673.1:g.8111685_8111700delinsGGGCGGCCCCGGAGCC	GRCh37
NC_000011.8:g.8068261_8068276delinsGGGCGGCCCCGGAGCC	NCBI36
NG_029912.1:g.56506_56521delinsGGGCGGCCCCGGAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.160_175delinsGGGCGGCCCCGGAGCC MANE Select	ENSP00000299506.3:p.Gly54=
ENST00000299506.2:c.160_175delinsGGGCGGCCCCGGAGCC	ENSP00000299506.2:p.Gly54=
ENST00000305253.8:c.325_340delinsGGGCGGCCCCGGAGCC	ENSP00000305426.4:p.Gly109=
ENST00000534099.5:c.178_193delinsGGGCGGCCCCGGAGCC	ENSP00000434400.1:p.Gly60=
NM_003320.4:c.325_340delinsGGGCGGCCCCGGAGCC	NP_003311.2:p.Gly109=
NM_177972.2:c.160_175delinsGGGCGGCCCCGGAGCC	NP_813977.1:p.Gly54=
XM_005253109.2:c.286_301delinsGGGCGGCCCCGGAGCC	XP_005253166.1:p.Gly96=
XM_011520344.1:c.196_211delinsGGGCGGCCCCGGAGCC	XP_011518646.1:p.Gly66=
XM_005253109.3:c.286_301delinsGGGCGGCCCCGGAGCC	XP_005253166.1:p.Gly96=
XM_011520344.2:c.196_211delinsGGGCGGCCCCGGAGCC	XP_011518646.1:p.Gly66=
NM_177972.3:c.160_175delinsGGGCGGCCCCGGAGCC MANE Select	NP_813977.1:p.Gly54=
NM_003320.5:c.325_340delinsGGGCGGCCCCGGAGCC	NP_003311.2:p.Gly109=