Canonical Allele Identifier: CA2790351814

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089829_8089834del , CM000673.2:g.8089829_8089834del	GRCh38
NC_000011.9:g.8111376_8111381del , CM000673.1:g.8111376_8111381del	GRCh37
NC_000011.8:g.8067952_8067957del	NCBI36
NG_029912.1:g.56197_56202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.90+168_90+173del MANE Select	ENSP00000299506.3:n.90+168_90+173del
ENST00000299506.2:c.90+168_90+173del	ENSP00000299506.2:n.90+168_90+173del
ENST00000305253.8:c.255+168_255+173del	ENSP00000305426.4:n.255+168_255+173del
ENST00000534099.5:c.108+168_108+173del	ENSP00000434400.1:n.108+168_108+173del
NM_003320.4:c.255+168_255+173del	NP_003311.2:n.255+168_255+173del
NM_177972.2:c.90+168_90+173del	NP_813977.1:n.90+168_90+173del
XM_005253109.2:c.216+168_216+173del	XP_005253166.1:n.216+168_216+173del
XM_011520344.1:c.126+168_126+173del	XP_011518646.1:n.126+168_126+173del
XM_005253109.3:c.216+168_216+173del	XP_005253166.1:n.216+168_216+173del
XM_011520344.2:c.126+168_126+173del	XP_011518646.1:n.126+168_126+173del
NM_177972.3:c.90+168_90+173del MANE Select	NP_813977.1:n.90+168_90+173del
NM_003320.5:c.255+168_255+173del	NP_003311.2:n.255+168_255+173del