Canonical Allele Identifier: CA1950952938

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089765G= , CM000673.2:g.8089765G=	GRCh38
NC_000011.9:g.8111312G= , CM000673.1:g.8111312G=	GRCh37
NC_000011.8:g.8067888G=	NCBI36
NG_029912.1:g.56133G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.90+104G= MANE Select	ENSP00000299506.3:n.90+104G=
ENST00000299506.2:c.90+104G=	ENSP00000299506.2:n.90+104G=
ENST00000305253.8:c.255+104G=	ENSP00000305426.4:n.255+104G=
ENST00000534099.5:c.108+104G=	ENSP00000434400.1:n.108+104G=
NM_003320.4:c.255+104G=	NP_003311.2:n.255+104G=
NM_177972.2:c.90+104G=	NP_813977.1:n.90+104G=
XM_005253109.2:c.216+104G=	XP_005253166.1:n.216+104G=
XM_011520344.1:c.126+104G=	XP_011518646.1:n.126+104G=
XM_005253109.3:c.216+104G=	XP_005253166.1:n.216+104G=
XM_011520344.2:c.126+104G=	XP_011518646.1:n.126+104G=
NM_177972.3:c.90+104G= MANE Select	NP_813977.1:n.90+104G=
NM_003320.5:c.255+104G=	NP_003311.2:n.255+104G=