Canonical Allele Identifier: CA3148151

Gene: TENM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.182738496A>G , CM000666.2:g.182738496A>G	GRCh38
NC_000004.11:g.183659649A>G , CM000666.1:g.183659649A>G	GRCh37
NC_000004.10:g.183896643A>G	NCBI36
NG_042859.1:g.500066A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000511685.6:c.3331A>G MANE Select	ENSP00000424226.1:p.Met1111Val
ENST00000406950.3:c.2821A>G	ENSP00000385276.3:p.Met941Val
ENST00000502950.1:n.1718A>G
ENST00000511685.5:c.3331A>G	ENSP00000424226.1:p.Met1111Val
NM_001080477.2:c.3331A>G	NP_001073946.1:p.Met1111Val
NM_001080477.3:c.3331A>G	NP_001073946.1:p.Met1111Val
XM_011532105.1:c.2560A>G	XP_011530407.1:p.Met854Val
XM_017008385.1:c.3358A>G	XP_016863874.1:p.Met1120Val
XM_017008386.1:c.3358A>G	XP_016863875.1:p.Met1120Val
XM_017008387.2:c.3358A>G	XP_016863876.1:p.Met1120Val
XM_017008388.1:c.3358A>G	XP_016863877.1:p.Met1120Val
XM_017008389.1:c.3358A>G	XP_016863878.1:p.Met1120Val
XM_017008390.1:c.3358A>G	XP_016863879.1:p.Met1120Val
XM_017008391.1:c.3358A>G	XP_016863880.1:p.Met1120Val
XM_017008392.1:c.3331A>G	XP_016863881.1:p.Met1111Val
XM_017008393.1:c.3331A>G	XP_016863882.1:p.Met1111Val
XM_017008394.1:c.3079A>G	XP_016863883.1:p.Met1027Val
XM_017008395.1:c.2866A>G	XP_016863884.1:p.Met956Val
XM_017008396.1:c.2542A>G	XP_016863885.1:p.Met848Val
NM_001080477.4:c.3331A>G MANE Select	NP_001073946.1:p.Met1111Val