Canonical Allele Identifier: CA1950953351

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090111C= , CM000673.2:g.8090111C=	GRCh38
NC_000011.9:g.8111658C= , CM000673.1:g.8111658C=	GRCh37
NC_000011.8:g.8068234C=	NCBI36
NG_029912.1:g.56479C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.133C= MANE Select	ENSP00000299506.3:p.Pro45=
ENST00000299506.2:c.133C=	ENSP00000299506.2:p.Pro45=
ENST00000305253.8:c.298C=	ENSP00000305426.4:p.Pro100=
ENST00000534099.5:c.151C=	ENSP00000434400.1:p.Pro51=
NM_003320.4:c.298C=	NP_003311.2:p.Pro100=
NM_177972.2:c.133C=	NP_813977.1:p.Pro45=
XM_005253109.2:c.259C=	XP_005253166.1:p.Pro87=
XM_011520344.1:c.169C=	XP_011518646.1:p.Pro57=
XM_005253109.3:c.259C=	XP_005253166.1:p.Pro87=
XM_011520344.2:c.169C=	XP_011518646.1:p.Pro57=
NM_177972.3:c.133C= MANE Select	NP_813977.1:p.Pro45=
NM_003320.5:c.298C=	NP_003311.2:p.Pro100=