Canonical Allele Identifier: CA2790351749

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089767_8089768insA , CM000673.2:g.8089767_8089768insA	GRCh38
NC_000011.9:g.8111314_8111315insA , CM000673.1:g.8111314_8111315insA	GRCh37
NC_000011.8:g.8067890_8067891insA	NCBI36
NG_029912.1:g.56135_56136insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.90+106_90+107insA MANE Select	ENSP00000299506.3:n.90+106_90+107insA
ENST00000299506.2:c.90+106_90+107insA	ENSP00000299506.2:n.90+106_90+107insA
ENST00000305253.8:c.255+106_255+107insA	ENSP00000305426.4:n.255+106_255+107insA
ENST00000534099.5:c.108+106_108+107insA	ENSP00000434400.1:n.108+106_108+107insA
NM_003320.4:c.255+106_255+107insA	NP_003311.2:n.255+106_255+107insA
NM_177972.2:c.90+106_90+107insA	NP_813977.1:n.90+106_90+107insA
XM_005253109.2:c.216+106_216+107insA	XP_005253166.1:n.216+106_216+107insA
XM_011520344.1:c.126+106_126+107insA	XP_011518646.1:n.126+106_126+107insA
XM_005253109.3:c.216+106_216+107insA	XP_005253166.1:n.216+106_216+107insA
XM_011520344.2:c.126+106_126+107insA	XP_011518646.1:n.126+106_126+107insA
NM_177972.3:c.90+106_90+107insA MANE Select	NP_813977.1:n.90+106_90+107insA
NM_003320.5:c.255+106_255+107insA	NP_003311.2:n.255+106_255+107insA