Canonical Allele Identifier: CA2790351824

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089830_8089831insAGTT , CM000673.2:g.8089830_8089831insAGTT	GRCh38
NC_000011.9:g.8111377_8111378insAGTT , CM000673.1:g.8111377_8111378insAGTT	GRCh37
NC_000011.8:g.8067953_8067954insAGTT	NCBI36
NG_029912.1:g.56198_56199insAGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.90+169_90+170insAGTT MANE Select	ENSP00000299506.3:n.90+169_90+170insAGTT
ENST00000299506.2:c.90+169_90+170insAGTT	ENSP00000299506.2:n.90+169_90+170insAGTT
ENST00000305253.8:c.255+169_255+170insAGTT	ENSP00000305426.4:n.255+169_255+170insAGTT
ENST00000534099.5:c.108+169_108+170insAGTT	ENSP00000434400.1:n.108+169_108+170insAGTT
NM_003320.4:c.255+169_255+170insAGTT	NP_003311.2:n.255+169_255+170insAGTT
NM_177972.2:c.90+169_90+170insAGTT	NP_813977.1:n.90+169_90+170insAGTT
XM_005253109.2:c.216+169_216+170insAGTT	XP_005253166.1:n.216+169_216+170insAGTT
XM_011520344.1:c.126+169_126+170insAGTT	XP_011518646.1:n.126+169_126+170insAGTT
XM_005253109.3:c.216+169_216+170insAGTT	XP_005253166.1:n.216+169_216+170insAGTT
XM_011520344.2:c.126+169_126+170insAGTT	XP_011518646.1:n.126+169_126+170insAGTT
NM_177972.3:c.90+169_90+170insAGTT MANE Select	NP_813977.1:n.90+169_90+170insAGTT
NM_003320.5:c.255+169_255+170insAGTT	NP_003311.2:n.255+169_255+170insAGTT