Canonical Allele Identifier: CA1950953106

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089934_8089936delinsCTT , CM000673.2:g.8089934_8089936delinsCTT	GRCh38
NC_000011.9:g.8111481_8111483delinsCTT , CM000673.1:g.8111481_8111483delinsCTT	GRCh37
NC_000011.8:g.8068057_8068059delinsCTT	NCBI36
NG_029912.1:g.56302_56304delinsCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.91-135_91-133delinsCTT MANE Select	ENSP00000299506.3:n.91-135_91-133delinsCT...
ENST00000299506.2:c.91-135_91-133delinsCTT	ENSP00000299506.2:n.91-135_91-133delinsCT...
ENST00000305253.8:c.256-135_256-133delinsCTT	ENSP00000305426.4:n.256-135_256-133delins...
ENST00000534099.5:c.109-135_109-133delinsCTT	ENSP00000434400.1:n.109-135_109-133delins...
NM_003320.4:c.256-135_256-133delinsCTT	NP_003311.2:n.256-135_256-133delinsCTT
NM_177972.2:c.91-135_91-133delinsCTT	NP_813977.1:n.91-135_91-133delinsCTT
XM_005253109.2:c.217-135_217-133delinsCTT	XP_005253166.1:n.217-135_217-133delinsCTT...
XM_011520344.1:c.127-135_127-133delinsCTT	XP_011518646.1:n.127-135_127-133delinsCTT...
XM_005253109.3:c.217-135_217-133delinsCTT	XP_005253166.1:n.217-135_217-133delinsCTT...
XM_011520344.2:c.127-135_127-133delinsCTT	XP_011518646.1:n.127-135_127-133delinsCTT...
NM_177972.3:c.91-135_91-133delinsCTT MANE Select	NP_813977.1:n.91-135_91-133delinsCTT
NM_003320.5:c.256-135_256-133delinsCTT	NP_003311.2:n.256-135_256-133delinsCTT