Canonical Allele Identifier: CA111752857

Gene: TENM3

Linked Data

• dbSNP Id: rs998177107
• gnomAD v3: 4-182766479-T-G
• gnomAD v4: 4-182766479-T-G
• MyVariant Identifiers: chr4:g.183687632T>G (hg19) ; chr4:g.182766479T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.182766479T>G , CM000666.2:g.182766479T>G	GRCh38
NC_000004.11:g.183687632T>G , CM000666.1:g.183687632T>G	GRCh37
NC_000004.10:g.183924626T>G	NCBI36
NG_042859.1:g.528049T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000511685.6:c.4893-6993T>G MANE Select	ENSP00000424226.1:n.4893-6993T>G
ENST00000406950.3:c.4383-6993T>G	ENSP00000385276.3:n.4383-6993T>G
ENST00000511685.5:c.4893-6993T>G	ENSP00000424226.1:n.4893-6993T>G
NM_001080477.2:c.4893-6993T>G	NP_001073946.1:n.4893-6993T>G
NM_001080477.3:c.4893-6993T>G	NP_001073946.1:n.4893-6993T>G
XM_011532105.1:c.4143-6993T>G	XP_011530407.1:n.4143-6993T>G
XR_939528.1:n.774-715A>C
XM_017008385.1:c.4941-6993T>G	XP_016863874.1:n.4941-6993T>G
XM_017008386.1:c.4941-6993T>G	XP_016863875.1:n.4941-6993T>G
XM_017008387.2:c.4941-6993T>G	XP_016863876.1:n.4941-6993T>G
XM_017008388.1:c.4941-6993T>G	XP_016863877.1:n.4941-6993T>G
XM_017008389.1:c.4938-6993T>G	XP_016863878.1:n.4938-6993T>G
XM_017008390.1:c.4920-6993T>G	XP_016863879.1:n.4920-6993T>G
XM_017008391.1:c.4917-6993T>G	XP_016863880.1:n.4917-6993T>G
XM_017008392.1:c.4914-6993T>G	XP_016863881.1:n.4914-6993T>G
XM_017008393.1:c.4893-6993T>G	XP_016863882.1:n.4893-6993T>G
XM_017008394.1:c.4662-6993T>G	XP_016863883.1:n.4662-6993T>G
XM_017008395.1:c.4449-6993T>G	XP_016863884.1:n.4449-6993T>G
XM_017008396.1:c.4125-6993T>G	XP_016863885.1:n.4125-6993T>G
XR_001741487.1:n.3996A>C
XR_939528.2:n.3262-715A>C
NM_001080477.4:c.4893-6993T>G MANE Select	NP_001073946.1:n.4893-6993T>G