Canonical Allele Identifier: CA111760421

Gene: TENM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.182729363C>T , CM000666.2:g.182729363C>T	GRCh38
NC_000004.11:g.183650516C>T , CM000666.1:g.183650516C>T	GRCh37
NC_000004.10:g.183887510C>T	NCBI36
NG_042859.1:g.490933C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001080477.4:c.2585+182C>T MANE Select	NP_001073946.1:n.2585+182C>T
ENST00000511685.6:c.2585+182C>T MANE Select	ENSP00000424226.1:n.2585+182C>T
NM_001080477.2:c.2585+182C>T	NP_001073946.1:n.2585+182C>T
NM_001080477.3:c.2585+182C>T	NP_001073946.1:n.2585+182C>T
ENST00000406950.3:c.2075+182C>T	ENSP00000385276.3:n.2075+182C>T
ENST00000502950.1:n.972+182C>T
ENST00000511685.5:c.2585+182C>T	ENSP00000424226.1:n.2585+182C>T
XM_011532105.1:c.1814+182C>T	XP_011530407.1:n.1814+182C>T
XM_017008385.1:c.2612+182C>T	XP_016863874.1:n.2612+182C>T
XM_017008386.1:c.2612+182C>T	XP_016863875.1:n.2612+182C>T
XM_017008387.2:c.2612+182C>T	XP_016863876.1:n.2612+182C>T
XM_017008388.1:c.2612+182C>T	XP_016863877.1:n.2612+182C>T
XM_017008389.1:c.2612+182C>T	XP_016863878.1:n.2612+182C>T
XM_017008390.1:c.2612+182C>T	XP_016863879.1:n.2612+182C>T
XM_017008391.1:c.2612+182C>T	XP_016863880.1:n.2612+182C>T
XM_017008392.1:c.2585+182C>T	XP_016863881.1:n.2585+182C>T
XM_017008393.1:c.2585+182C>T	XP_016863882.1:n.2585+182C>T
XM_017008394.1:c.2333+182C>T	XP_016863883.1:n.2333+182C>T
XM_017008395.1:c.2120+182C>T	XP_016863884.1:n.2120+182C>T
XM_017008396.1:c.1796+182C>T	XP_016863885.1:n.1796+182C>T