Canonical Allele Identifier: CA1950952633

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089550_8089551delinsTG , CM000673.2:g.8089550_8089551delinsTG	GRCh38
NC_000011.9:g.8111097_8111098delinsTG , CM000673.1:g.8111097_8111098delinsTG	GRCh37
NC_000011.8:g.8067673_8067674delinsTG	NCBI36
NG_029912.1:g.55918_55919delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39-60_39-59delinsTG MANE Select	ENSP00000299506.3:n.39-60_39-59delinsTG
ENST00000299506.2:c.39-60_39-59delinsTG	ENSP00000299506.2:n.39-60_39-59delinsTG
ENST00000305253.8:c.204-60_204-59delinsTG	ENSP00000305426.4:n.204-60_204-59delinsTG
ENST00000534099.5:c.57-60_57-59delinsTG	ENSP00000434400.1:n.57-60_57-59delinsTG
NM_003320.4:c.204-60_204-59delinsTG	NP_003311.2:n.204-60_204-59delinsTG
NM_177972.2:c.39-60_39-59delinsTG	NP_813977.1:n.39-60_39-59delinsTG
XM_005253109.2:c.165-60_165-59delinsTG	XP_005253166.1:n.165-60_165-59delinsTG
XM_011520344.1:c.75-60_75-59delinsTG	XP_011518646.1:n.75-60_75-59delinsTG
XM_005253109.3:c.165-60_165-59delinsTG	XP_005253166.1:n.165-60_165-59delinsTG
XM_011520344.2:c.75-60_75-59delinsTG	XP_011518646.1:n.75-60_75-59delinsTG
NM_177972.3:c.39-60_39-59delinsTG MANE Select	NP_813977.1:n.39-60_39-59delinsTG
NM_003320.5:c.204-60_204-59delinsTG	NP_003311.2:n.204-60_204-59delinsTG