Canonical Allele Identifier: CA2790351818

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089828_8089829insA , CM000673.2:g.8089828_8089829insA	GRCh38
NC_000011.9:g.8111375_8111376insA , CM000673.1:g.8111375_8111376insA	GRCh37
NC_000011.8:g.8067951_8067952insA	NCBI36
NG_029912.1:g.56196_56197insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.90+167_90+168insA MANE Select	ENSP00000299506.3:n.90+167_90+168insA
ENST00000299506.2:c.90+167_90+168insA	ENSP00000299506.2:n.90+167_90+168insA
ENST00000305253.8:c.255+167_255+168insA	ENSP00000305426.4:n.255+167_255+168insA
ENST00000534099.5:c.108+167_108+168insA	ENSP00000434400.1:n.108+167_108+168insA
NM_003320.4:c.255+167_255+168insA	NP_003311.2:n.255+167_255+168insA
NM_177972.2:c.90+167_90+168insA	NP_813977.1:n.90+167_90+168insA
XM_005253109.2:c.216+167_216+168insA	XP_005253166.1:n.216+167_216+168insA
XM_011520344.1:c.126+167_126+168insA	XP_011518646.1:n.126+167_126+168insA
XM_005253109.3:c.216+167_216+168insA	XP_005253166.1:n.216+167_216+168insA
XM_011520344.2:c.126+167_126+168insA	XP_011518646.1:n.126+167_126+168insA
NM_177972.3:c.90+167_90+168insA MANE Select	NP_813977.1:n.90+167_90+168insA
NM_003320.5:c.255+167_255+168insA	NP_003311.2:n.255+167_255+168insA