Canonical Allele Identifier: CA1950953497

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090163G= , CM000673.2:g.8090163G=	GRCh38
NC_000011.9:g.8111710G= , CM000673.1:g.8111710G=	GRCh37
NC_000011.8:g.8068286G=	NCBI36
NG_029912.1:g.56531G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.185G= MANE Select	ENSP00000299506.3:p.Arg62=
ENST00000299506.2:c.185G=	ENSP00000299506.2:p.Arg62=
ENST00000305253.8:c.350G=	ENSP00000305426.4:p.Arg117=
ENST00000534099.5:c.203G=	ENSP00000434400.1:p.Arg68=
NM_003320.4:c.350G=	NP_003311.2:p.Arg117=
NM_177972.2:c.185G=	NP_813977.1:p.Arg62=
XM_005253109.2:c.311G=	XP_005253166.1:p.Arg104=
XM_011520344.1:c.221G=	XP_011518646.1:p.Arg74=
XM_005253109.3:c.311G=	XP_005253166.1:p.Arg104=
XM_011520344.2:c.221G=	XP_011518646.1:p.Arg74=
NM_177972.3:c.185G= MANE Select	NP_813977.1:p.Arg62=
NM_003320.5:c.350G=	NP_003311.2:p.Arg117=