LDH info

Canonical Allele Identifier: CA658798616
Gene: CDH1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 516511

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68738288C>A , CM000678.2:g.68738288C>A GRCh38
NC_000016.9:g.68772191C>A , CM000678.1:g.68772191C>A GRCh37
NC_000016.8:g.67329692C>A NCBI36
NG_008021.1:g.5997C>A , LRG_301:g.5997C>A

Transcript Alleles

HGVS Amino-acid change
NM_004360.3:c.49-9C>A , LRG_301t1:c.49-9C>A NP_004351.1:p.=
NM_001317184.1:c.49-9C>A VV NP_001304113.1:p.=
NM_001317185.1:c.-1567-9C>A VV NP_001304114.1:p.=
NM_001317186.1:c.-1771-9C>A VV NP_001304115.1:p.=
NM_004360.4:c.49-9C>A VV NP_004351.1:p.=
NM_004360.5:c.49-9C>A VV MANE Preferred NP_004351.1:p.=
NM_001317184.2:c.49-9C>A VV NP_001304113.1:p.=
NM_001317185.2:c.-1567-9C>A VV NP_001304114.1:p.=
NM_001317186.2:c.-1771-9C>A VV NP_001304115.1:p.=
ENST00000261769.9:c.49-9C>A ENSP00000261769.4:p.=
ENST00000422392.6:c.49-9C>A ENSP00000414946.2:p.=
ENST00000566510.5:c.49-9C>A ENSP00000458139.1:p.=
ENST00000566612.5:c.49-9C>A ENSP00000454782.1:p.=
ENST00000611625.4:c.49-9C>A ENSP00000481063.1:p.=
ENST00000612417.4:c.49-9C>A ENSP00000478360.1:p.=
ENST00000621016.4:c.49-9C>A ENSP00000480664.1:p.=