Canonical Allele Identifier: CA1950952757

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089643G= , CM000673.2:g.8089643G=	GRCh38
NC_000011.9:g.8111190G= , CM000673.1:g.8111190G=	GRCh37
NC_000011.8:g.8067766G=	NCBI36
NG_029912.1:g.56011G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.72G= MANE Select	ENSP00000299506.3:p.Gln24=
ENST00000299506.2:c.72G=	ENSP00000299506.2:p.Gln24=
ENST00000305253.8:c.237G=	ENSP00000305426.4:p.Gln79=
ENST00000534099.5:c.90G=	ENSP00000434400.1:p.Gln30=
NM_003320.4:c.237G=	NP_003311.2:p.Gln79=
NM_177972.2:c.72G=	NP_813977.1:p.Gln24=
XM_005253109.2:c.198G=	XP_005253166.1:p.Gln66=
XM_011520344.1:c.108G=	XP_011518646.1:p.Gln36=
XM_005253109.3:c.198G=	XP_005253166.1:p.Gln66=
XM_011520344.2:c.108G=	XP_011518646.1:p.Gln36=
NM_177972.3:c.72G= MANE Select	NP_813977.1:p.Gln24=
NM_003320.5:c.237G=	NP_003311.2:p.Gln79=