Canonical Allele Identifier: CA2506065382

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089798_8089799del , CM000673.2:g.8089798_8089799del	GRCh38
NC_000011.9:g.8111345_8111346del , CM000673.1:g.8111345_8111346del	GRCh37
NC_000011.8:g.8067921_8067922del	NCBI36
NG_029912.1:g.56166_56167del

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.90+137_90+138del MANE Select	ENSP00000299506.3:n.90+137_90+138del
ENST00000299506.2:c.90+137_90+138del	ENSP00000299506.2:n.90+137_90+138del
ENST00000305253.8:c.255+137_255+138del	ENSP00000305426.4:n.255+137_255+138del
ENST00000534099.5:c.108+137_108+138del	ENSP00000434400.1:n.108+137_108+138del
NM_003320.4:c.255+137_255+138del	NP_003311.2:n.255+137_255+138del
NM_177972.2:c.90+137_90+138del	NP_813977.1:n.90+137_90+138del
XM_005253109.2:c.216+137_216+138del	XP_005253166.1:n.216+137_216+138del
XM_011520344.1:c.126+137_126+138del	XP_011518646.1:n.126+137_126+138del
XM_005253109.3:c.216+137_216+138del	XP_005253166.1:n.216+137_216+138del
XM_011520344.2:c.126+137_126+138del	XP_011518646.1:n.126+137_126+138del
NM_177972.3:c.90+137_90+138del MANE Select	NP_813977.1:n.90+137_90+138del
NM_003320.5:c.255+137_255+138del	NP_003311.2:n.255+137_255+138del