Canonical Allele Identifier: CA2790351829

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089831_8089832insAG , CM000673.2:g.8089831_8089832insAG	GRCh38
NC_000011.9:g.8111378_8111379insAG , CM000673.1:g.8111378_8111379insAG	GRCh37
NC_000011.8:g.8067954_8067955insAG	NCBI36
NG_029912.1:g.56199_56200insAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.90+170_90+171insAG MANE Select	ENSP00000299506.3:n.90+170_90+171insAG
ENST00000299506.2:c.90+170_90+171insAG	ENSP00000299506.2:n.90+170_90+171insAG
ENST00000305253.8:c.255+170_255+171insAG	ENSP00000305426.4:n.255+170_255+171insAG
ENST00000534099.5:c.108+170_108+171insAG	ENSP00000434400.1:n.108+170_108+171insAG
NM_003320.4:c.255+170_255+171insAG	NP_003311.2:n.255+170_255+171insAG
NM_177972.2:c.90+170_90+171insAG	NP_813977.1:n.90+170_90+171insAG
XM_005253109.2:c.216+170_216+171insAG	XP_005253166.1:n.216+170_216+171insAG
XM_011520344.1:c.126+170_126+171insAG	XP_011518646.1:n.126+170_126+171insAG
XM_005253109.3:c.216+170_216+171insAG	XP_005253166.1:n.216+170_216+171insAG
XM_011520344.2:c.126+170_126+171insAG	XP_011518646.1:n.126+170_126+171insAG
NM_177972.3:c.90+170_90+171insAG MANE Select	NP_813977.1:n.90+170_90+171insAG
NM_003320.5:c.255+170_255+171insAG	NP_003311.2:n.255+170_255+171insAG