Canonical Allele Identifier: CA2790351849

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089844_8089845insA , CM000673.2:g.8089844_8089845insA	GRCh38
NC_000011.9:g.8111391_8111392insA , CM000673.1:g.8111391_8111392insA	GRCh37
NC_000011.8:g.8067967_8067968insA	NCBI36
NG_029912.1:g.56212_56213insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.90+183_90+184insA MANE Select	ENSP00000299506.3:n.90+183_90+184insA
ENST00000299506.2:c.90+183_90+184insA	ENSP00000299506.2:n.90+183_90+184insA
ENST00000305253.8:c.255+183_255+184insA	ENSP00000305426.4:n.255+183_255+184insA
ENST00000534099.5:c.108+183_108+184insA	ENSP00000434400.1:n.108+183_108+184insA
NM_003320.4:c.255+183_255+184insA	NP_003311.2:n.255+183_255+184insA
NM_177972.2:c.90+183_90+184insA	NP_813977.1:n.90+183_90+184insA
XM_005253109.2:c.216+183_216+184insA	XP_005253166.1:n.216+183_216+184insA
XM_011520344.1:c.126+183_126+184insA	XP_011518646.1:n.126+183_126+184insA
XM_005253109.3:c.216+183_216+184insA	XP_005253166.1:n.216+183_216+184insA
XM_011520344.2:c.126+183_126+184insA	XP_011518646.1:n.126+183_126+184insA
NM_177972.3:c.90+183_90+184insA MANE Select	NP_813977.1:n.90+183_90+184insA
NM_003320.5:c.255+183_255+184insA	NP_003311.2:n.255+183_255+184insA