Canonical Allele Identifier: CA1950952878

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089727_8089728delinsAG , CM000673.2:g.8089727_8089728delinsAG	GRCh38
NC_000011.9:g.8111274_8111275delinsAG , CM000673.1:g.8111274_8111275delinsAG	GRCh37
NC_000011.8:g.8067850_8067851delinsAG	NCBI36
NG_029912.1:g.56095_56096delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.90+66_90+67delinsAG MANE Select	ENSP00000299506.3:n.90+66_90+67delinsAG
ENST00000299506.2:c.90+66_90+67delinsAG	ENSP00000299506.2:n.90+66_90+67delinsAG
ENST00000305253.8:c.255+66_255+67delinsAG	ENSP00000305426.4:n.255+66_255+67delinsAG
ENST00000534099.5:c.108+66_108+67delinsAG	ENSP00000434400.1:n.108+66_108+67delinsAG
NM_003320.4:c.255+66_255+67delinsAG	NP_003311.2:n.255+66_255+67delinsAG
NM_177972.2:c.90+66_90+67delinsAG	NP_813977.1:n.90+66_90+67delinsAG
XM_005253109.2:c.216+66_216+67delinsAG	XP_005253166.1:n.216+66_216+67delinsAG
XM_011520344.1:c.126+66_126+67delinsAG	XP_011518646.1:n.126+66_126+67delinsAG
XM_005253109.3:c.216+66_216+67delinsAG	XP_005253166.1:n.216+66_216+67delinsAG
XM_011520344.2:c.126+66_126+67delinsAG	XP_011518646.1:n.126+66_126+67delinsAG
NM_177972.3:c.90+66_90+67delinsAG MANE Select	NP_813977.1:n.90+66_90+67delinsAG
NM_003320.5:c.255+66_255+67delinsAG	NP_003311.2:n.255+66_255+67delinsAG