Canonical Allele Identifier: CA2790351875

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089888_8089893del , CM000673.2:g.8089888_8089893del	GRCh38
NC_000011.9:g.8111435_8111440del , CM000673.1:g.8111435_8111440del	GRCh37
NC_000011.8:g.8068011_8068016del	NCBI36
NG_029912.1:g.56256_56261del

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.91-181_91-176del MANE Select	ENSP00000299506.3:n.91-181_91-176del
ENST00000299506.2:c.91-181_91-176del	ENSP00000299506.2:n.91-181_91-176del
ENST00000305253.8:c.256-181_256-176del	ENSP00000305426.4:n.256-181_256-176del
ENST00000534099.5:c.109-181_109-176del	ENSP00000434400.1:n.109-181_109-176del
NM_003320.4:c.256-181_256-176del	NP_003311.2:n.256-181_256-176del
NM_177972.2:c.91-181_91-176del	NP_813977.1:n.91-181_91-176del
XM_005253109.2:c.217-181_217-176del	XP_005253166.1:n.217-181_217-176del
XM_011520344.1:c.127-181_127-176del	XP_011518646.1:n.127-181_127-176del
XM_005253109.3:c.217-181_217-176del	XP_005253166.1:n.217-181_217-176del
XM_011520344.2:c.127-181_127-176del	XP_011518646.1:n.127-181_127-176del
NM_177972.3:c.91-181_91-176del MANE Select	NP_813977.1:n.91-181_91-176del
NM_003320.5:c.256-181_256-176del	NP_003311.2:n.256-181_256-176del