Canonical Allele Identifier: CA1950953481

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090159_8090160delinsGC , CM000673.2:g.8090159_8090160delinsGC	GRCh38
NC_000011.9:g.8111706_8111707delinsGC , CM000673.1:g.8111706_8111707delinsGC	GRCh37
NC_000011.8:g.8068282_8068283delinsGC	NCBI36
NG_029912.1:g.56527_56528delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.181_182delinsGC MANE Select	ENSP00000299506.3:p.Ala61=
ENST00000299506.2:c.181_182delinsGC	ENSP00000299506.2:p.Ala61=
ENST00000305253.8:c.346_347delinsGC	ENSP00000305426.4:p.Ala116=
ENST00000534099.5:c.199_200delinsGC	ENSP00000434400.1:p.Ala67=
NM_003320.4:c.346_347delinsGC	NP_003311.2:p.Ala116=
NM_177972.2:c.181_182delinsGC	NP_813977.1:p.Ala61=
XM_005253109.2:c.307_308delinsGC	XP_005253166.1:p.Ala103=
XM_011520344.1:c.217_218delinsGC	XP_011518646.1:p.Ala73=
XM_005253109.3:c.307_308delinsGC	XP_005253166.1:p.Ala103=
XM_011520344.2:c.217_218delinsGC	XP_011518646.1:p.Ala73=
NM_177972.3:c.181_182delinsGC MANE Select	NP_813977.1:p.Ala61=
NM_003320.5:c.346_347delinsGC	NP_003311.2:p.Ala116=