Canonical Allele Identifier: CA279900
Gene: LRPPRC HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 218166
ClinVar RCV Id: RCV000202390
dbSNP Id: rs863225444

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43934787_43934789del , CM000664.2:g.43934787_43934789del GRCh38
NC_000002.11:g.44161926_44161928del , CM000664.1:g.44161926_44161928del GRCh37
NC_000002.10:g.44015430_44015432del NCBI36
NG_008247.1:g.66218_66220del

Transcript Alleles

HGVS Amino-acid change
NM_133259.3:c.2595_2597del VV NP_573566.2:p.Val866del
XM_006711915.2:c.2517_2519del XP_006711978.1:p.Val840del
XM_006711916.2:c.2595_2597del XP_006711979.1:p.Val866del
XM_011532473.1:c.2595_2597del XP_011530775.1:p.Val866del
XM_011532474.1:c.2595_2597del XP_011530776.1:p.Val866del
XM_006711916.3:c.2595_2597del XP_006711979.1:p.Val866del
XM_017003117.1:c.2517_2519del XP_016858606.1:p.Val840del
XR_002958896.1:n.2637_2639del
NM_133259.4:c.2595_2597del VV MANE Preferred NP_573566.2:p.Val866del
ENST00000260665.11:c.2595_2597del ENSP00000260665.7:p.Val866del