Canonical Allele Identifier: CA3148314

Gene: TENM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.182752070T>A , CM000666.2:g.182752070T>A	GRCh38
NC_000004.11:g.183673223T>A , CM000666.1:g.183673223T>A	GRCh37
NC_000004.10:g.183910217T>A	NCBI36
NG_042859.1:g.513640T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001080477.4:c.3862+38T>A MANE Select	NP_001073946.1:n.3862+38T>A
ENST00000511685.6:c.3862+38T>A MANE Select	ENSP00000424226.1:n.3862+38T>A
NM_001080477.2:c.3862+38T>A	NP_001073946.1:n.3862+38T>A
NM_001080477.3:c.3862+38T>A	NP_001073946.1:n.3862+38T>A
ENST00000406950.3:c.3352+38T>A	ENSP00000385276.3:n.3352+38T>A
ENST00000502950.1:n.2270+38T>A
ENST00000511685.5:c.3862+38T>A	ENSP00000424226.1:n.3862+38T>A
XM_011532105.1:c.3112+38T>A	XP_011530407.1:n.3112+38T>A
XM_017008385.1:c.3910+38T>A	XP_016863874.1:n.3910+38T>A
XM_017008386.1:c.3910+38T>A	XP_016863875.1:n.3910+38T>A
XM_017008387.2:c.3910+38T>A	XP_016863876.1:n.3910+38T>A
XM_017008388.1:c.3910+38T>A	XP_016863877.1:n.3910+38T>A
XM_017008389.1:c.3907+38T>A	XP_016863878.1:n.3907+38T>A
XM_017008390.1:c.3889+38T>A	XP_016863879.1:n.3889+38T>A
XM_017008391.1:c.3886+38T>A	XP_016863880.1:n.3886+38T>A
XM_017008392.1:c.3883+38T>A	XP_016863881.1:n.3883+38T>A
XM_017008393.1:c.3862+38T>A	XP_016863882.1:n.3862+38T>A
XM_017008394.1:c.3631+38T>A	XP_016863883.1:n.3631+38T>A
XM_017008395.1:c.3418+38T>A	XP_016863884.1:n.3418+38T>A
XM_017008396.1:c.3094+38T>A	XP_016863885.1:n.3094+38T>A