Canonical Allele Identifier: CA217415589

Gene: TUB

Linked Data

• dbSNP Id: rs866605659

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090148_8090149delinsAA , CM000673.2:g.8090148_8090149delinsAA	GRCh38
NC_000011.9:g.8111695_8111696delinsAA , CM000673.1:g.8111695_8111696delinsAA	GRCh37
NC_000011.8:g.8068271_8068272delinsAA	NCBI36
NG_029912.1:g.56516_56517delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.170_171delinsAA MANE Select	ENSP00000299506.3:p.Arg57Gln
ENST00000299506.2:c.170_171delinsAA	ENSP00000299506.2:p.Arg57Gln
ENST00000305253.8:c.335_336delinsAA	ENSP00000305426.4:p.Arg112Gln
ENST00000534099.5:c.188_189delinsAA	ENSP00000434400.1:p.Arg63Gln
NM_003320.4:c.335_336delinsAA	NP_003311.2:p.Arg112Gln
NM_177972.2:c.170_171delinsAA	NP_813977.1:p.Arg57Gln
XM_005253109.2:c.296_297delinsAA	XP_005253166.1:p.Arg99Gln
XM_011520344.1:c.206_207delinsAA	XP_011518646.1:p.Arg69Gln
XM_005253109.3:c.296_297delinsAA	XP_005253166.1:p.Arg99Gln
XM_011520344.2:c.206_207delinsAA	XP_011518646.1:p.Arg69Gln
NM_177972.3:c.170_171delinsAA MANE Select	NP_813977.1:p.Arg57Gln
NM_003320.5:c.335_336delinsAA	NP_003311.2:p.Arg112Gln