Canonical Allele Identifier: CA2790351757

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089780_8089781insACT , CM000673.2:g.8089780_8089781insACT	GRCh38
NC_000011.9:g.8111327_8111328insACT , CM000673.1:g.8111327_8111328insACT	GRCh37
NC_000011.8:g.8067903_8067904insACT	NCBI36
NG_029912.1:g.56148_56149insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.90+119_90+120insACT MANE Select	ENSP00000299506.3:n.90+119_90+120insACT
ENST00000299506.2:c.90+119_90+120insACT	ENSP00000299506.2:n.90+119_90+120insACT
ENST00000305253.8:c.255+119_255+120insACT	ENSP00000305426.4:n.255+119_255+120insACT
ENST00000534099.5:c.108+119_108+120insACT	ENSP00000434400.1:n.108+119_108+120insACT
NM_003320.4:c.255+119_255+120insACT	NP_003311.2:n.255+119_255+120insACT
NM_177972.2:c.90+119_90+120insACT	NP_813977.1:n.90+119_90+120insACT
XM_005253109.2:c.216+119_216+120insACT	XP_005253166.1:n.216+119_216+120insACT
XM_011520344.1:c.126+119_126+120insACT	XP_011518646.1:n.126+119_126+120insACT
XM_005253109.3:c.216+119_216+120insACT	XP_005253166.1:n.216+119_216+120insACT
XM_011520344.2:c.126+119_126+120insACT	XP_011518646.1:n.126+119_126+120insACT
NM_177972.3:c.90+119_90+120insACT MANE Select	NP_813977.1:n.90+119_90+120insACT
NM_003320.5:c.255+119_255+120insACT	NP_003311.2:n.255+119_255+120insACT