LDH info

Canonical Allele Identifier: CA11859448
Gene: TENM3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10017238

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.182766636T>C , CM000666.2:g.182766636T>C GRCh38
NC_000004.11:g.183687789T>C , CM000666.1:g.183687789T>C GRCh37
NC_000004.10:g.183924783T>C NCBI36
NG_042859.1:g.528206T>C

Transcript Alleles

HGVS Amino-acid change
NM_001080477.2:c.4893-6836T>C VV NP_001073946.1:p.=
NM_001080477.3:c.4893-6836T>C VV NP_001073946.1:p.=
XM_011532105.1:c.4143-6836T>C XP_011530407.1:p.=
XR_939528.1:n.773+578A>G
XM_017008385.1:c.4941-6836T>C XP_016863874.1:p.=
XM_017008386.1:c.4941-6836T>C XP_016863875.1:p.=
XM_017008387.2:c.4941-6836T>C XP_016863876.1:p.=
XM_017008388.1:c.4941-6836T>C XP_016863877.1:p.=
XM_017008389.1:c.4938-6836T>C XP_016863878.1:p.=
XM_017008390.1:c.4920-6836T>C XP_016863879.1:p.=
XM_017008391.1:c.4917-6836T>C XP_016863880.1:p.=
XM_017008392.1:c.4914-6836T>C XP_016863881.1:p.=
XM_017008393.1:c.4893-6836T>C XP_016863882.1:p.=
XM_017008394.1:c.4662-6836T>C XP_016863883.1:p.=
XM_017008395.1:c.4449-6836T>C XP_016863884.1:p.=
XM_017008396.1:c.4125-6836T>C XP_016863885.1:p.=
XR_001741487.1:n.3839A>G
XR_939528.2:n.3261+578A>G
NM_001080477.4:c.4893-6836T>C VV MANE Preferred NP_001073946.1:p.=
ENST00000406950.3:n.4383-6836T>C ENSP00000385276.3:p.=
ENST00000511685.5:c.4893-6836T>C ENSP00000424226.1:p.=