Canonical Allele Identifier: CA2699650758
Gene: WDPCP HGNC NCBI

Linked Data

dbSNP Id: rs2105190828

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.63404445del , CM000664.2:g.63404445del GRCh38
NC_000002.11:g.63631580del , CM000664.1:g.63631580del GRCh37
NC_000002.10:g.63485084del NCBI36
NG_028144.1:g.189288del
NG_028144.2:g.441381del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272321.12:c.1038del MANE Select ENSP00000272321.7:p.Asn346LysfsTer7
ENST00000272321.11:c.1038del ENSP00000272321.7:p.Asn346LysfsTer7
ENST00000398544.7:c.561del ENSP00000381552.3:p.Asn187LysfsTer7
ENST00000409120.5:c.462del ENSP00000386769.1:p.Asn154LysfsTer7
ENST00000409199.5:c.462del ENSP00000386592.1:p.Asn154LysfsTer7
ENST00000409354.6:c.399del ENSP00000386795.2:p.Asn133LysfsTer7
ENST00000409562.7:c.1038del ENSP00000387222.3:p.Asn346LysfsTer7
ENST00000409835.5:n.1285del
ENST00000417238.5:c.*1149del ENSP00000411429.1:n.*1149del
ENST00000493315.1:n.740del
NM_001042692.2:c.561del NP_001036157.1:p.Asn187LysfsTer7
NM_015910.5:c.1038del NP_056994.3:p.Asn346LysfsTer7
NR_122106.1:n.685del
XM_005264348.2:c.1038del XP_005264405.1:p.Asn346LysfsTer7
XM_011532881.1:c.966del XP_011531183.1:p.Asn322LysfsTer7
XM_011532882.1:c.939del XP_011531184.1:p.Asn313LysfsTer7
XM_011532883.1:c.1038del XP_011531185.1:p.Asn346LysfsTer7
XM_011532884.1:c.1038del XP_011531186.1:p.Asn346LysfsTer7
XM_011532885.1:c.1038del XP_011531187.1:p.Asn346LysfsTer7
XM_011532886.1:c.1038del XP_011531188.1:p.Asn346LysfsTer7
XM_011532887.1:c.1038del XP_011531189.1:p.Asn346LysfsTer7
XM_011532888.1:c.1038del XP_011531190.1:p.Asn346LysfsTer7
XM_011532889.1:c.1038del XP_011531191.1:p.Asn346LysfsTer7
XM_011532890.1:c.1038del XP_011531192.1:p.Asn346LysfsTer7
XM_011532891.1:c.966del XP_011531193.1:p.Asn322LysfsTer7
XR_244934.1:n.1285del
XR_244935.1:n.1285del
XR_939686.1:n.1285del
NM_001042692.3:c.561del NP_001036157.1:p.Asn187LysfsTer7
NM_001354044.1:c.966del NP_001340973.1:p.Asn322LysfsTer7
NM_001354045.1:c.1038del NP_001340974.1:p.Asn346LysfsTer7
NM_015910.6:c.1038del NP_056994.3:p.Asn346LysfsTer7
NR_122106.2:n.685del
NR_148704.1:n.1818del
NR_148705.1:n.1566del
XM_005264348.4:c.1038del XP_005264405.1:p.Asn346LysfsTer7
XM_011532881.3:c.966del XP_011531183.1:p.Asn322LysfsTer7
XM_011532884.3:c.1038del XP_011531186.1:p.Asn346LysfsTer7
XM_011532887.3:c.1038del XP_011531189.1:p.Asn346LysfsTer7
XM_011532890.3:c.1038del XP_011531192.1:p.Asn346LysfsTer7
XM_011532891.2:c.966del XP_011531193.1:p.Asn322LysfsTer7
XM_017004253.2:c.1038del XP_016859742.1:p.Asn346LysfsTer7
XM_017004254.2:c.1038del XP_016859743.1:p.Asn346LysfsTer7
XR_001738759.2:n.1500del
XR_001738760.2:n.1500del
XR_002959303.1:n.1500del
XR_244934.3:n.1500del
NM_015910.7:c.1038del MANE Select NP_056994.3:p.Asn346LysfsTer7
NM_001354044.2:c.966del NP_001340973.1:p.Asn322LysfsTer7
NM_001354045.2:c.1038del NP_001340974.1:p.Asn346LysfsTer7
NR_148704.2:n.1496del
NR_148705.2:n.1244del