LDH info

Canonical Allele Identifier: CA15996971
Gene: CHEK2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs5762746

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28692135T>C , CM000684.2:g.28692135T>C GRCh38
NC_000022.10:g.29088123T>C , CM000684.1:g.29088123T>C GRCh37
NC_000022.9:g.27418123T>C NCBI36
NG_008150.1:g.54700A>G
NG_008150.2:g.54732A>G

Transcript Alleles

HGVS Amino-acid change
NM_001005735.1:c.1590+1897A>G VV NP_001005735.1:p.=
NM_001257387.1:c.798+1897A>G VV NP_001244316.1:p.=
NM_007194.3:c.1461+1897A>G VV NP_009125.1:p.=
NM_145862.2:c.1374+1897A>G VV NP_665861.1:p.=
XM_006724114.2:c.981+1897A>G XP_006724177.1:p.=
XM_006724116.2:c.918+1897A>G XP_006724179.2:p.=
XM_011529839.1:n.1620+1897A>G XP_011528141.1:p.=
XM_011529840.1:c.1533+1897A>G XP_011528142.1:p.=
XM_011529841.1:c.1389+1897A>G XP_011528143.1:p.=
XM_011529842.1:n.1290+1897A>G XP_011528144.1:p.=
XM_011529843.1:c.1260+1897A>G XP_011528145.1:p.=
XM_011529845.1:c.798+1897A>G XP_011528147.1:p.=
XR_937805.1:n.1620+1897A>G
NM_001349956.1:c.1260+1897A>G VV NP_001336885.1:p.=
NM_007194.4:c.1461+1897A>G VV MANE Preferred NP_009125.1:p.=
XM_006724114.3:c.1014+1897A>G XP_006724177.2:p.=
XM_011529839.2:c.1620+1897A>G XP_011528141.1:p.=
XM_011529840.3:c.1533+1897A>G XP_011528142.1:p.=
XM_011529842.2:c.1290+1897A>G XP_011528144.1:p.=
XM_011529845.2:c.798+1897A>G XP_011528147.1:p.=
XM_017028560.1:c.1584+1897A>G XP_016884049.1:p.=
XM_017028561.2:c.798+1897A>G XP_016884050.1:p.=
XM_024452148.1:c.1491+1897A>G XP_024307916.1:p.=
XM_024452149.1:c.1404+1897A>G XP_024307917.1:p.=
XR_937805.2:n.1631+1897A>G
NM_001005735.2:c.1590+1897A>G VV NP_001005735.1:p.=
NM_001257387.2:c.798+1897A>G VV NP_001244316.1:p.=
NM_001349956.2:c.1260+1897A>G VV NP_001336885.1:p.=
ENST00000328354.10:c.1461+1897A>G ENSP00000329178.6:p.=
ENST00000348295.7:c.1374+1897A>G ENSP00000329012.5:p.=
ENST00000382580.6:c.1590+1897A>G ENSP00000372023.2:p.=
ENST00000402731.5:n.1374+1897A>G ENSP00000384835.1:p.=
ENST00000403642.5:n.1188+1897A>G ENSP00000384919.1:p.=
ENST00000404276.5:n.1461+1897A>G ENSP00000385747.1:p.=
ENST00000405598.5:c.1461+1897A>G ENSP00000386087.1:p.=
ENST00000416671.5:c.*951+1897A>G ENSP00000402225.1:p.=
ENST00000417588.5:n.1370+1897A>G ENSP00000412901.1:p.=
ENST00000433728.5:n.1399+1897A>G ENSP00000404400.1:p.=
ENST00000434810.5:n.659+1897A>G
ENST00000448511.5:n.1351+1897A>G ENSP00000404567.1:p.=
ENST00000456369.5:n.264-2920A>G