Canonical Allele Identifier: CA1518208826

Gene: TENM3

Linked Data

• dbSNP Id: rs10013166

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.182556176G>C , CM000666.2:g.182556176G>C	GRCh38
NC_000004.11:g.183477329G>C , CM000666.1:g.183477329G>C	GRCh37
NC_000004.10:g.183714323G>C	NCBI36
NG_042859.1:g.317746G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000511685.6:c.512-44748G>C MANE Select	ENSP00000424226.1:n.512-44748G>C
ENST00000510504.1:c.86-44748G>C	ENSP00000426914.1:n.86-44748G>C
ENST00000511685.5:c.512-44748G>C	ENSP00000424226.1:n.512-44748G>C
NM_001080477.2:c.512-44748G>C	NP_001073946.1:n.512-44748G>C
NM_001080477.3:c.512-44748G>C	NP_001073946.1:n.512-44748G>C
XM_011532105.1:c.-305-44748G>C	XP_011530407.1:n.-305-44748G>C
XM_017008385.1:c.512-44748G>C	XP_016863874.1:n.512-44748G>C
XM_017008386.1:c.512-44748G>C	XP_016863875.1:n.512-44748G>C
XM_017008387.2:c.512-44748G>C	XP_016863876.1:n.512-44748G>C
XM_017008388.1:c.512-44748G>C	XP_016863877.1:n.512-44748G>C
XM_017008389.1:c.512-44748G>C	XP_016863878.1:n.512-44748G>C
XM_017008390.1:c.512-44748G>C	XP_016863879.1:n.512-44748G>C
XM_017008391.1:c.512-44748G>C	XP_016863880.1:n.512-44748G>C
XM_017008392.1:c.512-44748G>C	XP_016863881.1:n.512-44748G>C
XM_017008393.1:c.512-44748G>C	XP_016863882.1:n.512-44748G>C
XM_017008394.1:c.233-44748G>C	XP_016863883.1:n.233-44748G>C
XM_017008395.1:c.20-44748G>C	XP_016863884.1:n.20-44748G>C
XM_017008396.1:c.-305-44748G>C	XP_016863885.1:n.-305-44748G>C
NM_001080477.4:c.512-44748G>C MANE Select	NP_001073946.1:n.512-44748G>C