Canonical Allele Identifier: CA2790351839

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089840_8089841insAGT , CM000673.2:g.8089840_8089841insAGT	GRCh38
NC_000011.9:g.8111387_8111388insAGT , CM000673.1:g.8111387_8111388insAGT	GRCh37
NC_000011.8:g.8067963_8067964insAGT	NCBI36
NG_029912.1:g.56208_56209insAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.90+179_90+180insAGT MANE Select	ENSP00000299506.3:n.90+179_90+180insAGT
ENST00000299506.2:c.90+179_90+180insAGT	ENSP00000299506.2:n.90+179_90+180insAGT
ENST00000305253.8:c.255+179_255+180insAGT	ENSP00000305426.4:n.255+179_255+180insAGT
ENST00000534099.5:c.108+179_108+180insAGT	ENSP00000434400.1:n.108+179_108+180insAGT
NM_003320.4:c.255+179_255+180insAGT	NP_003311.2:n.255+179_255+180insAGT
NM_177972.2:c.90+179_90+180insAGT	NP_813977.1:n.90+179_90+180insAGT
XM_005253109.2:c.216+179_216+180insAGT	XP_005253166.1:n.216+179_216+180insAGT
XM_011520344.1:c.126+179_126+180insAGT	XP_011518646.1:n.126+179_126+180insAGT
XM_005253109.3:c.216+179_216+180insAGT	XP_005253166.1:n.216+179_216+180insAGT
XM_011520344.2:c.126+179_126+180insAGT	XP_011518646.1:n.126+179_126+180insAGT
NM_177972.3:c.90+179_90+180insAGT MANE Select	NP_813977.1:n.90+179_90+180insAGT
NM_003320.5:c.255+179_255+180insAGT	NP_003311.2:n.255+179_255+180insAGT