Canonical Allele Identifier: CA1950952981

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089800_8089802delinsACT , CM000673.2:g.8089800_8089802delinsACT	GRCh38
NC_000011.9:g.8111347_8111349delinsACT , CM000673.1:g.8111347_8111349delinsACT	GRCh37
NC_000011.8:g.8067923_8067925delinsACT	NCBI36
NG_029912.1:g.56168_56170delinsACT

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.90+139_90+141delinsACT MANE Select	ENSP00000299506.3:n.90+139_90+141delinsAC...
ENST00000299506.2:c.90+139_90+141delinsACT	ENSP00000299506.2:n.90+139_90+141delinsAC...
ENST00000305253.8:c.255+139_255+141delinsACT	ENSP00000305426.4:n.255+139_255+141delins...
ENST00000534099.5:c.108+139_108+141delinsACT	ENSP00000434400.1:n.108+139_108+141delins...
NM_003320.4:c.255+139_255+141delinsACT	NP_003311.2:n.255+139_255+141delinsACT
NM_177972.2:c.90+139_90+141delinsACT	NP_813977.1:n.90+139_90+141delinsACT
XM_005253109.2:c.216+139_216+141delinsACT	XP_005253166.1:n.216+139_216+141delinsACT...
XM_011520344.1:c.126+139_126+141delinsACT	XP_011518646.1:n.126+139_126+141delinsACT...
XM_005253109.3:c.216+139_216+141delinsACT	XP_005253166.1:n.216+139_216+141delinsACT...
XM_011520344.2:c.126+139_126+141delinsACT	XP_011518646.1:n.126+139_126+141delinsACT...
NM_177972.3:c.90+139_90+141delinsACT MANE Select	NP_813977.1:n.90+139_90+141delinsACT
NM_003320.5:c.255+139_255+141delinsACT	NP_003311.2:n.255+139_255+141delinsACT