Canonical Allele Identifier: CA792005259

Gene: TENM3

Linked Data

• dbSNP Id: rs1269624245
• gnomAD v3: 4-182766604-G-C
• gnomAD v4: 4-182766604-G-C
• MyVariant Identifiers: chr4:g.183687757G>C (hg19) ; chr4:g.182766604G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.182766604G>C , CM000666.2:g.182766604G>C	GRCh38
NC_000004.11:g.183687757G>C , CM000666.1:g.183687757G>C	GRCh37
NC_000004.10:g.183924751G>C	NCBI36
NG_042859.1:g.528174G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000511685.6:c.4893-6868G>C MANE Select	ENSP00000424226.1:n.4893-6868G>C
ENST00000406950.3:c.4383-6868G>C	ENSP00000385276.3:n.4383-6868G>C
ENST00000511685.5:c.4893-6868G>C	ENSP00000424226.1:n.4893-6868G>C
NM_001080477.2:c.4893-6868G>C	NP_001073946.1:n.4893-6868G>C
NM_001080477.3:c.4893-6868G>C	NP_001073946.1:n.4893-6868G>C
XM_011532105.1:c.4143-6868G>C	XP_011530407.1:n.4143-6868G>C
XR_939528.1:n.773+610C>G
XM_017008385.1:c.4941-6868G>C	XP_016863874.1:n.4941-6868G>C
XM_017008386.1:c.4941-6868G>C	XP_016863875.1:n.4941-6868G>C
XM_017008387.2:c.4941-6868G>C	XP_016863876.1:n.4941-6868G>C
XM_017008388.1:c.4941-6868G>C	XP_016863877.1:n.4941-6868G>C
XM_017008389.1:c.4938-6868G>C	XP_016863878.1:n.4938-6868G>C
XM_017008390.1:c.4920-6868G>C	XP_016863879.1:n.4920-6868G>C
XM_017008391.1:c.4917-6868G>C	XP_016863880.1:n.4917-6868G>C
XM_017008392.1:c.4914-6868G>C	XP_016863881.1:n.4914-6868G>C
XM_017008393.1:c.4893-6868G>C	XP_016863882.1:n.4893-6868G>C
XM_017008394.1:c.4662-6868G>C	XP_016863883.1:n.4662-6868G>C
XM_017008395.1:c.4449-6868G>C	XP_016863884.1:n.4449-6868G>C
XM_017008396.1:c.4125-6868G>C	XP_016863885.1:n.4125-6868G>C
XR_001741487.1:n.3871C>G
XR_939528.2:n.3261+610C>G
NM_001080477.4:c.4893-6868G>C MANE Select	NP_001073946.1:n.4893-6868G>C