Canonical Allele Identifier: CA1518305320

Gene: TENM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.182766560T= , CM000666.2:g.182766560T=	GRCh38
NC_000004.11:g.183687713T= , CM000666.1:g.183687713T=	GRCh37
NC_000004.10:g.183924707T=	NCBI36
NG_042859.1:g.528130T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000511685.6:c.4893-6912T= MANE Select	ENSP00000424226.1:n.4893-6912T=
ENST00000406950.3:c.4383-6912T=	ENSP00000385276.3:n.4383-6912T=
ENST00000511685.5:c.4893-6912T=	ENSP00000424226.1:n.4893-6912T=
NM_001080477.2:c.4893-6912T=	NP_001073946.1:n.4893-6912T=
NM_001080477.3:c.4893-6912T=	NP_001073946.1:n.4893-6912T=
XM_011532105.1:c.4143-6912T=	XP_011530407.1:n.4143-6912T=
XR_939528.1:n.773+654A=
XM_017008385.1:c.4941-6912T=	XP_016863874.1:n.4941-6912T=
XM_017008386.1:c.4941-6912T=	XP_016863875.1:n.4941-6912T=
XM_017008387.2:c.4941-6912T=	XP_016863876.1:n.4941-6912T=
XM_017008388.1:c.4941-6912T=	XP_016863877.1:n.4941-6912T=
XM_017008389.1:c.4938-6912T=	XP_016863878.1:n.4938-6912T=
XM_017008390.1:c.4920-6912T=	XP_016863879.1:n.4920-6912T=
XM_017008391.1:c.4917-6912T=	XP_016863880.1:n.4917-6912T=
XM_017008392.1:c.4914-6912T=	XP_016863881.1:n.4914-6912T=
XM_017008393.1:c.4893-6912T=	XP_016863882.1:n.4893-6912T=
XM_017008394.1:c.4662-6912T=	XP_016863883.1:n.4662-6912T=
XM_017008395.1:c.4449-6912T=	XP_016863884.1:n.4449-6912T=
XM_017008396.1:c.4125-6912T=	XP_016863885.1:n.4125-6912T=
XR_001741487.1:n.3915A=
XR_939528.2:n.3261+654A=
NM_001080477.4:c.4893-6912T= MANE Select	NP_001073946.1:n.4893-6912T=