Canonical Allele Identifier: CA3147516

Gene: TENM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.182628678T>G , CM000666.2:g.182628678T>G	GRCh38
NC_000004.11:g.183549831T>G , CM000666.1:g.183549831T>G	GRCh37
NC_000004.10:g.183786825T>G	NCBI36
NG_042859.1:g.390248T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000511685.6:c.777T>G MANE Select	ENSP00000424226.1:p.Gly259=
ENST00000406950.3:c.267T>G	ENSP00000385276.3:p.Gly89=
ENST00000510504.1:c.351T>G	ENSP00000426914.1:p.Gly117=
ENST00000511685.5:c.777T>G	ENSP00000424226.1:p.Gly259=
NM_001080477.2:c.777T>G	NP_001073946.1:p.Gly259=
NM_001080477.3:c.777T>G	NP_001073946.1:p.Gly259=
XM_011532105.1:c.-40T>G	XP_011530407.1:n.-40T>G
XM_017008385.1:c.777T>G	XP_016863874.1:p.Gly259=
XM_017008386.1:c.777T>G	XP_016863875.1:p.Gly259=
XM_017008387.2:c.777T>G	XP_016863876.1:p.Gly259=
XM_017008388.1:c.777T>G	XP_016863877.1:p.Gly259=
XM_017008389.1:c.777T>G	XP_016863878.1:p.Gly259=
XM_017008390.1:c.777T>G	XP_016863879.1:p.Gly259=
XM_017008391.1:c.777T>G	XP_016863880.1:p.Gly259=
XM_017008392.1:c.777T>G	XP_016863881.1:p.Gly259=
XM_017008393.1:c.777T>G	XP_016863882.1:p.Gly259=
XM_017008394.1:c.498T>G	XP_016863883.1:p.Gly166=
XM_017008395.1:c.285T>G	XP_016863884.1:p.Gly95=
XM_017008396.1:c.-40T>G	XP_016863885.1:n.-40T>G
NM_001080477.4:c.777T>G MANE Select	NP_001073946.1:p.Gly259=