Canonical Allele Identifier: CA1950952831

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089698_8089699delinsTG , CM000673.2:g.8089698_8089699delinsTG	GRCh38
NC_000011.9:g.8111245_8111246delinsTG , CM000673.1:g.8111245_8111246delinsTG	GRCh37
NC_000011.8:g.8067821_8067822delinsTG	NCBI36
NG_029912.1:g.56066_56067delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.90+37_90+38delinsTG MANE Select	ENSP00000299506.3:n.90+37_90+38delinsTG
ENST00000299506.2:c.90+37_90+38delinsTG	ENSP00000299506.2:n.90+37_90+38delinsTG
ENST00000305253.8:c.255+37_255+38delinsTG	ENSP00000305426.4:n.255+37_255+38delinsTG
ENST00000534099.5:c.108+37_108+38delinsTG	ENSP00000434400.1:n.108+37_108+38delinsTG
NM_003320.4:c.255+37_255+38delinsTG	NP_003311.2:n.255+37_255+38delinsTG
NM_177972.2:c.90+37_90+38delinsTG	NP_813977.1:n.90+37_90+38delinsTG
XM_005253109.2:c.216+37_216+38delinsTG	XP_005253166.1:n.216+37_216+38delinsTG
XM_011520344.1:c.126+37_126+38delinsTG	XP_011518646.1:n.126+37_126+38delinsTG
XM_005253109.3:c.216+37_216+38delinsTG	XP_005253166.1:n.216+37_216+38delinsTG
XM_011520344.2:c.126+37_126+38delinsTG	XP_011518646.1:n.126+37_126+38delinsTG
NM_177972.3:c.90+37_90+38delinsTG MANE Select	NP_813977.1:n.90+37_90+38delinsTG
NM_003320.5:c.255+37_255+38delinsTG	NP_003311.2:n.255+37_255+38delinsTG