Canonical Allele Identifier: CA1950953312

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090092G= , CM000673.2:g.8090092G=	GRCh38
NC_000011.9:g.8111639G= , CM000673.1:g.8111639G=	GRCh37
NC_000011.8:g.8068215G=	NCBI36
NG_029912.1:g.56460G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.114G= MANE Select	ENSP00000299506.3:p.Gln38=
ENST00000299506.2:c.114G=	ENSP00000299506.2:p.Gln38=
ENST00000305253.8:c.279G=	ENSP00000305426.4:p.Gln93=
ENST00000534099.5:c.132G=	ENSP00000434400.1:p.Gln44=
NM_003320.4:c.279G=	NP_003311.2:p.Gln93=
NM_177972.2:c.114G=	NP_813977.1:p.Gln38=
XM_005253109.2:c.240G=	XP_005253166.1:p.Gln80=
XM_011520344.1:c.150G=	XP_011518646.1:p.Gln50=
XM_005253109.3:c.240G=	XP_005253166.1:p.Gln80=
XM_011520344.2:c.150G=	XP_011518646.1:p.Gln50=
NM_177972.3:c.114G= MANE Select	NP_813977.1:p.Gln38=
NM_003320.5:c.279G=	NP_003311.2:p.Gln93=