Canonical Allele Identifier: CA1950952760

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089647A= , CM000673.2:g.8089647A=	GRCh38
NC_000011.9:g.8111194A= , CM000673.1:g.8111194A=	GRCh37
NC_000011.8:g.8067770A=	NCBI36
NG_029912.1:g.56015A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.76A= MANE Select	ENSP00000299506.3:p.Lys26=
ENST00000299506.2:c.76A=	ENSP00000299506.2:p.Lys26=
ENST00000305253.8:c.241A=	ENSP00000305426.4:p.Lys81=
ENST00000534099.5:c.94A=	ENSP00000434400.1:p.Lys32=
NM_003320.4:c.241A=	NP_003311.2:p.Lys81=
NM_177972.2:c.76A=	NP_813977.1:p.Lys26=
XM_005253109.2:c.202A=	XP_005253166.1:p.Lys68=
XM_011520344.1:c.112A=	XP_011518646.1:p.Lys38=
XM_005253109.3:c.202A=	XP_005253166.1:p.Lys68=
XM_011520344.2:c.112A=	XP_011518646.1:p.Lys38=
NM_177972.3:c.76A= MANE Select	NP_813977.1:p.Lys26=
NM_003320.5:c.241A=	NP_003311.2:p.Lys81=