Canonical Allele Identifier: CA2790351865

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089869_8089870del , CM000673.2:g.8089869_8089870del	GRCh38
NC_000011.9:g.8111416_8111417del , CM000673.1:g.8111416_8111417del	GRCh37
NC_000011.8:g.8067992_8067993del	NCBI36
NG_029912.1:g.56237_56238del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.91-200_91-199del MANE Select	ENSP00000299506.3:n.91-200_91-199del
ENST00000299506.2:c.91-200_91-199del	ENSP00000299506.2:n.91-200_91-199del
ENST00000305253.8:c.256-200_256-199del	ENSP00000305426.4:n.256-200_256-199del
ENST00000534099.5:c.109-200_109-199del	ENSP00000434400.1:n.109-200_109-199del
NM_003320.4:c.256-200_256-199del	NP_003311.2:n.256-200_256-199del
NM_177972.2:c.91-200_91-199del	NP_813977.1:n.91-200_91-199del
XM_005253109.2:c.217-200_217-199del	XP_005253166.1:n.217-200_217-199del
XM_011520344.1:c.127-200_127-199del	XP_011518646.1:n.127-200_127-199del
XM_005253109.3:c.217-200_217-199del	XP_005253166.1:n.217-200_217-199del
XM_011520344.2:c.127-200_127-199del	XP_011518646.1:n.127-200_127-199del
NM_177972.3:c.91-200_91-199del MANE Select	NP_813977.1:n.91-200_91-199del
NM_003320.5:c.256-200_256-199del	NP_003311.2:n.256-200_256-199del