Canonical Allele Identifier: CA3147626

Gene: TENM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.182673122T>C , CM000666.2:g.182673122T>C	GRCh38
NC_000004.11:g.183594275T>C , CM000666.1:g.183594275T>C	GRCh37
NC_000004.10:g.183831269T>C	NCBI36
NG_042859.1:g.434692T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000511685.6:c.1229T>C MANE Select	ENSP00000424226.1:p.Ile410Thr
ENST00000406950.3:c.719T>C	ENSP00000385276.3:p.Ile240Thr
ENST00000511685.5:c.1229T>C	ENSP00000424226.1:p.Ile410Thr
NM_001080477.2:c.1229T>C	NP_001073946.1:p.Ile410Thr
NM_001080477.3:c.1229T>C	NP_001073946.1:p.Ile410Thr
XM_011532105.1:c.413T>C	XP_011530407.1:p.Ile138Thr
XM_017008385.1:c.1229T>C	XP_016863874.1:p.Ile410Thr
XM_017008386.1:c.1229T>C	XP_016863875.1:p.Ile410Thr
XM_017008387.2:c.1229T>C	XP_016863876.1:p.Ile410Thr
XM_017008388.1:c.1229T>C	XP_016863877.1:p.Ile410Thr
XM_017008389.1:c.1229T>C	XP_016863878.1:p.Ile410Thr
XM_017008390.1:c.1229T>C	XP_016863879.1:p.Ile410Thr
XM_017008391.1:c.1229T>C	XP_016863880.1:p.Ile410Thr
XM_017008392.1:c.1229T>C	XP_016863881.1:p.Ile410Thr
XM_017008393.1:c.1229T>C	XP_016863882.1:p.Ile410Thr
XM_017008394.1:c.950T>C	XP_016863883.1:p.Ile317Thr
XM_017008395.1:c.737T>C	XP_016863884.1:p.Ile246Thr
XM_017008396.1:c.413T>C	XP_016863885.1:p.Ile138Thr
NM_001080477.4:c.1229T>C MANE Select	NP_001073946.1:p.Ile410Thr