Canonical Allele Identifier: CA1950952971

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089796G= , CM000673.2:g.8089796G=	GRCh38
NC_000011.9:g.8111343G= , CM000673.1:g.8111343G=	GRCh37
NC_000011.8:g.8067919G=	NCBI36
NG_029912.1:g.56164G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.90+135G= MANE Select	ENSP00000299506.3:n.90+135G=
ENST00000299506.2:c.90+135G=	ENSP00000299506.2:n.90+135G=
ENST00000305253.8:c.255+135G=	ENSP00000305426.4:n.255+135G=
ENST00000534099.5:c.108+135G=	ENSP00000434400.1:n.108+135G=
NM_003320.4:c.255+135G=	NP_003311.2:n.255+135G=
NM_177972.2:c.90+135G=	NP_813977.1:n.90+135G=
XM_005253109.2:c.216+135G=	XP_005253166.1:n.216+135G=
XM_011520344.1:c.126+135G=	XP_011518646.1:n.126+135G=
XM_005253109.3:c.216+135G=	XP_005253166.1:n.216+135G=
XM_011520344.2:c.126+135G=	XP_011518646.1:n.126+135G=
NM_177972.3:c.90+135G= MANE Select	NP_813977.1:n.90+135G=
NM_003320.5:c.255+135G=	NP_003311.2:n.255+135G=