LDH info

Canonical Allele Identifier: CA14957296
Gene: CHEK2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4035540

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28691053T>C , CM000684.2:g.28691053T>C GRCh38
NC_000022.10:g.29087041T>C , CM000684.1:g.29087041T>C GRCh37
NC_000022.9:g.27417041T>C NCBI36
NG_008150.1:g.55782A>G
NG_008150.2:g.55814A>G

Transcript Alleles

HGVS Amino-acid change
NM_001005735.1:c.1591-1838A>G VV NP_001005735.1:p.=
NM_001257387.1:c.799-1838A>G VV NP_001244316.1:p.=
NM_007194.3:c.1462-1838A>G VV NP_009125.1:p.=
NM_145862.2:c.1375-1838A>G VV NP_665861.1:p.=
XM_006724114.2:c.982-1838A>G XP_006724177.1:p.=
XM_006724116.2:c.919-1838A>G XP_006724179.2:p.=
XM_011529839.1:n.1621-1838A>G XP_011528141.1:p.=
XM_011529840.1:c.1534-1838A>G XP_011528142.1:p.=
XM_011529841.1:c.1390-1838A>G XP_011528143.1:p.=
XM_011529842.1:n.1291-1838A>G XP_011528144.1:p.=
XM_011529843.1:c.1261-1838A>G XP_011528145.1:p.=
XM_011529845.1:c.799-1838A>G XP_011528147.1:p.=
XR_937805.1:n.1621-1838A>G
NM_001349956.1:c.1261-1838A>G VV NP_001336885.1:p.=
NM_007194.4:c.1462-1838A>G VV MANE Preferred NP_009125.1:p.=
XM_006724114.3:c.1015-1838A>G XP_006724177.2:p.=
XM_011529839.2:c.1621-1838A>G XP_011528141.1:p.=
XM_011529840.3:c.1534-1838A>G XP_011528142.1:p.=
XM_011529842.2:c.1291-1838A>G XP_011528144.1:p.=
XM_011529845.2:c.799-1838A>G XP_011528147.1:p.=
XM_017028560.1:c.1585-1838A>G XP_016884049.1:p.=
XM_017028561.2:c.799-1838A>G XP_016884050.1:p.=
XM_024452148.1:c.1492-1838A>G XP_024307916.1:p.=
XM_024452149.1:c.1405-1838A>G XP_024307917.1:p.=
XR_937805.2:n.1632-1838A>G
ENST00000328354.10:c.1462-1838A>G ENSP00000329178.6:p.=
ENST00000348295.7:c.1375-1838A>G ENSP00000329012.5:p.=
ENST00000382580.6:c.1591-1838A>G ENSP00000372023.2:p.=
ENST00000402731.5:n.1375-1838A>G ENSP00000384835.1:p.=
ENST00000403642.5:n.1189-1838A>G ENSP00000384919.1:p.=
ENST00000404276.5:n.1462-1838A>G ENSP00000385747.1:p.=
ENST00000405598.5:c.1462-1838A>G ENSP00000386087.1:p.=
ENST00000416671.5:c.*952-1838A>G ENSP00000402225.1:p.=
ENST00000417588.5:n.1371-1838A>G ENSP00000412901.1:p.=
ENST00000433728.5:n.1400-1838A>G ENSP00000404400.1:p.=
ENST00000434810.5:n.660-1838A>G
ENST00000448511.5:n.1352-1838A>G ENSP00000404567.1:p.=
ENST00000456369.5:n.264-1838A>G