LDH info

Canonical Allele Identifier: CA115501
Gene: PLCE1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 18423
ClinVar RCV Id: RCV000002443
dbSNP Id: rs267606954

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94032007C>T , CM000672.2:g.94032007C>T GRCh38
NC_000010.10:g.95791764C>T , CM000672.1:g.95791764C>T GRCh37
NC_000010.9:g.95781754C>T NCBI36
NG_015799.1:g.43019C>T

Transcript Alleles

HGVS Amino-acid change
NM_001288989.1:c.961C>T VV NP_001275918.1:p.Arg321Ter
NM_016341.3:c.961C>T VV NP_057425.3:p.Arg321Ter
XM_006717885.2:c.961C>T XP_006717948.1:p.Arg321Ter
XM_006717886.2:c.961C>T XP_006717949.1:p.Arg321Ter
XM_006717888.2:c.961C>T XP_006717951.1:p.Arg321Ter
XM_006717889.2:c.961C>T XP_006717952.1:p.Arg321Ter
XM_011539849.1:c.961C>T XP_011538151.1:p.Arg321Ter
XM_011539851.1:c.961C>T XP_011538153.1:p.Arg321Ter
XM_011539852.1:c.961C>T XP_011538154.1:p.Arg321Ter
XM_006717885.4:c.961C>T XP_006717948.1:p.Arg321Ter
XM_006717888.4:c.961C>T XP_006717951.1:p.Arg321Ter
XM_006717889.4:c.961C>T XP_006717952.1:p.Arg321Ter
XM_011539849.3:c.961C>T XP_011538151.1:p.Arg321Ter
XM_011539851.3:c.961C>T XP_011538153.1:p.Arg321Ter
XM_011539852.3:c.961C>T XP_011538154.1:p.Arg321Ter
XM_017016310.2:c.961C>T XP_016871799.1:p.Arg321Ter
XM_017016311.2:c.961C>T XP_016871800.1:p.Arg321Ter
NM_001288989.2:c.961C>T VV NP_001275918.1:p.Arg321Ter
NM_016341.4:c.961C>T VV MANE Preferred NP_057425.3:p.Arg321Ter
ENST00000260766.7:c.961C>T ENSP00000260766.3:p.Arg321Ter
ENST00000371380.7:c.961C>T ENSP00000360431.2:p.Arg321Ter