Canonical Allele Identifier: CA2790351752

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089771_8089772insA , CM000673.2:g.8089771_8089772insA	GRCh38
NC_000011.9:g.8111318_8111319insA , CM000673.1:g.8111318_8111319insA	GRCh37
NC_000011.8:g.8067894_8067895insA	NCBI36
NG_029912.1:g.56139_56140insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.90+110_90+111insA MANE Select	ENSP00000299506.3:n.90+110_90+111insA
ENST00000299506.2:c.90+110_90+111insA	ENSP00000299506.2:n.90+110_90+111insA
ENST00000305253.8:c.255+110_255+111insA	ENSP00000305426.4:n.255+110_255+111insA
ENST00000534099.5:c.108+110_108+111insA	ENSP00000434400.1:n.108+110_108+111insA
NM_003320.4:c.255+110_255+111insA	NP_003311.2:n.255+110_255+111insA
NM_177972.2:c.90+110_90+111insA	NP_813977.1:n.90+110_90+111insA
XM_005253109.2:c.216+110_216+111insA	XP_005253166.1:n.216+110_216+111insA
XM_011520344.1:c.126+110_126+111insA	XP_011518646.1:n.126+110_126+111insA
XM_005253109.3:c.216+110_216+111insA	XP_005253166.1:n.216+110_216+111insA
XM_011520344.2:c.126+110_126+111insA	XP_011518646.1:n.126+110_126+111insA
NM_177972.3:c.90+110_90+111insA MANE Select	NP_813977.1:n.90+110_90+111insA
NM_003320.5:c.255+110_255+111insA	NP_003311.2:n.255+110_255+111insA