LDH info

Canonical Allele Identifier: CA16042157
Gene: CDH1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 371806
dbSNP Id: rs1057517542

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829653G>A , CM000678.2:g.68829653G>A GRCh38
NC_000016.9:g.68863556G>A , CM000678.1:g.68863556G>A GRCh37
NC_000016.8:g.67421057G>A NCBI36
NG_008021.1:g.97362G>A , LRG_301:g.97362G>A

Transcript Alleles

HGVS Amino-acid change
NM_004360.3:c.2296-1G>A , LRG_301t1:c.2296-1G>A NP_004351.1:p.=
XM_011523488.1:c.1561-1G>A XP_011521790.1:p.=
XM_011523489.1:c.1561-1G>A XP_011521791.1:p.=
NM_001317184.1:c.2113-1G>A VV NP_001304113.1:p.=
NM_001317185.1:c.748-1G>A VV NP_001304114.1:p.=
NM_001317186.1:c.331-1G>A VV NP_001304115.1:p.=
NM_004360.4:c.2296-1G>A VV NP_004351.1:p.=
NM_004360.5:c.2296-1G>A VV MANE Preferred NP_004351.1:p.=
ENST00000261769.9:c.2296-1G>A ENSP00000261769.4:p.=
ENST00000422392.6:c.2113-1G>A ENSP00000414946.2:p.=
ENST00000562118.1:n.514-1G>A
ENST00000562836.5:n.2367-1G>A
ENST00000566510.5:c.*962-1G>A ENSP00000458139.1:p.=
ENST00000566612.5:c.*536-1G>A ENSP00000454782.1:p.=
ENST00000611625.4:c.2359-1G>A ENSP00000481063.1:p.=
ENST00000612417.4:c.1853+3099G>A ENSP00000478360.1:p.=
ENST00000621016.4:c.1866-4550G>A ENSP00000480664.1:p.=