Canonical Allele Identifier: CA1950952869

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089721_8089722delinsAG , CM000673.2:g.8089721_8089722delinsAG	GRCh38
NC_000011.9:g.8111268_8111269delinsAG , CM000673.1:g.8111268_8111269delinsAG	GRCh37
NC_000011.8:g.8067844_8067845delinsAG	NCBI36
NG_029912.1:g.56089_56090delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.90+60_90+61delinsAG MANE Select	ENSP00000299506.3:n.90+60_90+61delinsAG
ENST00000299506.2:c.90+60_90+61delinsAG	ENSP00000299506.2:n.90+60_90+61delinsAG
ENST00000305253.8:c.255+60_255+61delinsAG	ENSP00000305426.4:n.255+60_255+61delinsAG
ENST00000534099.5:c.108+60_108+61delinsAG	ENSP00000434400.1:n.108+60_108+61delinsAG
NM_003320.4:c.255+60_255+61delinsAG	NP_003311.2:n.255+60_255+61delinsAG
NM_177972.2:c.90+60_90+61delinsAG	NP_813977.1:n.90+60_90+61delinsAG
XM_005253109.2:c.216+60_216+61delinsAG	XP_005253166.1:n.216+60_216+61delinsAG
XM_011520344.1:c.126+60_126+61delinsAG	XP_011518646.1:n.126+60_126+61delinsAG
XM_005253109.3:c.216+60_216+61delinsAG	XP_005253166.1:n.216+60_216+61delinsAG
XM_011520344.2:c.126+60_126+61delinsAG	XP_011518646.1:n.126+60_126+61delinsAG
NM_177972.3:c.90+60_90+61delinsAG MANE Select	NP_813977.1:n.90+60_90+61delinsAG
NM_003320.5:c.255+60_255+61delinsAG	NP_003311.2:n.255+60_255+61delinsAG