Canonical Allele Identifier: CA112260453

Gene: TENM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.182601267_182601269del , CM000666.2:g.182601267_182601269del	GRCh38
NC_000004.11:g.183522420_183522422del , CM000666.1:g.183522420_183522422del	GRCh37
NC_000004.10:g.183759414_183759416del	NCBI36
NG_042859.1:g.362837_362839del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000511685.6:c.749+106_749+108del MANE Select	ENSP00000424226.1:n.749+106_749+108del
ENST00000406950.3:c.239+106_239+108del	ENSP00000385276.3:n.239+106_239+108del
ENST00000510504.1:c.323+106_323+108del	ENSP00000426914.1:n.323+106_323+108del
ENST00000511685.5:c.749+106_749+108del	ENSP00000424226.1:n.749+106_749+108del
NM_001080477.2:c.749+106_749+108del	NP_001073946.1:n.749+106_749+108del
NM_001080477.3:c.749+106_749+108del	NP_001073946.1:n.749+106_749+108del
XM_011532105.1:c.-68+106_-68+108del	XP_011530407.1:n.-68+106_-68+108del
XM_017008385.1:c.749+106_749+108del	XP_016863874.1:n.749+106_749+108del
XM_017008386.1:c.749+106_749+108del	XP_016863875.1:n.749+106_749+108del
XM_017008387.2:c.749+106_749+108del	XP_016863876.1:n.749+106_749+108del
XM_017008388.1:c.749+106_749+108del	XP_016863877.1:n.749+106_749+108del
XM_017008389.1:c.749+106_749+108del	XP_016863878.1:n.749+106_749+108del
XM_017008390.1:c.749+106_749+108del	XP_016863879.1:n.749+106_749+108del
XM_017008391.1:c.749+106_749+108del	XP_016863880.1:n.749+106_749+108del
XM_017008392.1:c.749+106_749+108del	XP_016863881.1:n.749+106_749+108del
XM_017008393.1:c.749+106_749+108del	XP_016863882.1:n.749+106_749+108del
XM_017008394.1:c.470+106_470+108del	XP_016863883.1:n.470+106_470+108del
XM_017008395.1:c.257+106_257+108del	XP_016863884.1:n.257+106_257+108del
XM_017008396.1:c.-68+106_-68+108del	XP_016863885.1:n.-68+106_-68+108del
NM_001080477.4:c.749+106_749+108del MANE Select	NP_001073946.1:n.749+106_749+108del