Canonical Allele Identifier: CA11741166

Gene: TENM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.182680945C>G , CM000666.2:g.182680945C>G	GRCh38
NC_000004.11:g.183602098C>G , CM000666.1:g.183602098C>G	GRCh37
NC_000004.10:g.183839092C>G	NCBI36
NG_042859.1:g.442515C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001080477.4:c.1834+208C>G MANE Select	NP_001073946.1:n.1834+208C>G
ENST00000511685.6:c.1834+208C>G MANE Select	ENSP00000424226.1:n.1834+208C>G
NM_001080477.2:c.1834+208C>G	NP_001073946.1:n.1834+208C>G
NM_001080477.3:c.1834+208C>G	NP_001073946.1:n.1834+208C>G
ENST00000406950.3:c.1324+208C>G	ENSP00000385276.3:n.1324+208C>G
ENST00000502950.1:n.221+208C>G
ENST00000507737.1:n.366+208C>G
ENST00000511685.5:c.1834+208C>G	ENSP00000424226.1:n.1834+208C>G
XM_011532105.1:c.1018+208C>G	XP_011530407.1:n.1018+208C>G
XM_017008385.1:c.1834+208C>G	XP_016863874.1:n.1834+208C>G
XM_017008386.1:c.1834+208C>G	XP_016863875.1:n.1834+208C>G
XM_017008387.2:c.1834+208C>G	XP_016863876.1:n.1834+208C>G
XM_017008388.1:c.1834+208C>G	XP_016863877.1:n.1834+208C>G
XM_017008389.1:c.1834+208C>G	XP_016863878.1:n.1834+208C>G
XM_017008390.1:c.1834+208C>G	XP_016863879.1:n.1834+208C>G
XM_017008391.1:c.1834+208C>G	XP_016863880.1:n.1834+208C>G
XM_017008392.1:c.1834+208C>G	XP_016863881.1:n.1834+208C>G
XM_017008393.1:c.1834+208C>G	XP_016863882.1:n.1834+208C>G
XM_017008394.1:c.1555+208C>G	XP_016863883.1:n.1555+208C>G
XM_017008395.1:c.1342+208C>G	XP_016863884.1:n.1342+208C>G
XM_017008396.1:c.1018+208C>G	XP_016863885.1:n.1018+208C>G