Canonical Allele Identifier: CA2790351746

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089762_8089767del , CM000673.2:g.8089762_8089767del	GRCh38
NC_000011.9:g.8111309_8111314del , CM000673.1:g.8111309_8111314del	GRCh37
NC_000011.8:g.8067885_8067890del	NCBI36
NG_029912.1:g.56130_56135del

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.90+101_90+106del MANE Select	ENSP00000299506.3:n.90+101_90+106del
ENST00000299506.2:c.90+101_90+106del	ENSP00000299506.2:n.90+101_90+106del
ENST00000305253.8:c.255+101_255+106del	ENSP00000305426.4:n.255+101_255+106del
ENST00000534099.5:c.108+101_108+106del	ENSP00000434400.1:n.108+101_108+106del
NM_003320.4:c.255+101_255+106del	NP_003311.2:n.255+101_255+106del
NM_177972.2:c.90+101_90+106del	NP_813977.1:n.90+101_90+106del
XM_005253109.2:c.216+101_216+106del	XP_005253166.1:n.216+101_216+106del
XM_011520344.1:c.126+101_126+106del	XP_011518646.1:n.126+101_126+106del
XM_005253109.3:c.216+101_216+106del	XP_005253166.1:n.216+101_216+106del
XM_011520344.2:c.126+101_126+106del	XP_011518646.1:n.126+101_126+106del
NM_177972.3:c.90+101_90+106del MANE Select	NP_813977.1:n.90+101_90+106del
NM_003320.5:c.255+101_255+106del	NP_003311.2:n.255+101_255+106del