Canonical Allele Identifier: CA2576983686

Gene: WDPCP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.63404343del , CM000664.2:g.63404343del	GRCh38
NC_000002.11:g.63631478del , CM000664.1:g.63631478del	GRCh37
NC_000002.10:g.63484982del	NCBI36
NG_028144.1:g.189391del
NG_028144.2:g.441484del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272321.12:c.1141del MANE Select	ENSP00000272321.7:p.Ser381HisfsTer2
ENST00000272321.11:c.1141del	ENSP00000272321.7:p.Ser381HisfsTer2
ENST00000398544.7:c.664del	ENSP00000381552.3:p.Ser222HisfsTer2
ENST00000409120.5:c.565del	ENSP00000386769.1:p.Ser189HisfsTer2
ENST00000409199.5:c.565del	ENSP00000386592.1:p.Ser189HisfsTer2
ENST00000409354.6:c.502del	ENSP00000386795.2:p.Ser168HisfsTer2
ENST00000409562.7:c.1141del	ENSP00000387222.3:p.Ser381HisfsTer2
ENST00000409835.5:n.1388del
ENST00000417238.5:c.*1252del	ENSP00000411429.1:n.*1252del
ENST00000493315.1:n.843del
NM_001042692.2:c.664del	NP_001036157.1:p.Ser222HisfsTer2
NM_015910.5:c.1141del	NP_056994.3:p.Ser381HisfsTer2
NR_122106.1:n.788del
XM_005264348.2:c.1141del	XP_005264405.1:p.Ser381HisfsTer2
XM_011532881.1:c.1069del	XP_011531183.1:p.Ser357HisfsTer2
XM_011532882.1:c.1042del	XP_011531184.1:p.Ser348HisfsTer2
XM_011532883.1:c.1141del	XP_011531185.1:p.Ser381HisfsTer2
XM_011532884.1:c.1141del	XP_011531186.1:p.Ser381HisfsTer2
XM_011532885.1:c.1141del	XP_011531187.1:p.Ser381HisfsTer2
XM_011532886.1:c.1141del	XP_011531188.1:p.Ser381HisfsTer2
XM_011532887.1:c.1141del	XP_011531189.1:p.Ser381HisfsTer2
XM_011532888.1:c.1141del	XP_011531190.1:p.Ser381HisfsTer2
XM_011532889.1:c.1141del	XP_011531191.1:p.Ser381HisfsTer2
XM_011532890.1:c.1141del	XP_011531192.1:p.Ser381HisfsTer2
XM_011532891.1:c.1069del	XP_011531193.1:p.Ser357HisfsTer2
XR_244934.1:n.1388del
XR_244935.1:n.1388del
XR_939686.1:n.1388del
NM_001042692.3:c.664del	NP_001036157.1:p.Ser222HisfsTer2
NM_001354044.1:c.1069del	NP_001340973.1:p.Ser357HisfsTer2
NM_001354045.1:c.1141del	NP_001340974.1:p.Ser381HisfsTer2
NM_015910.6:c.1141del	NP_056994.3:p.Ser381HisfsTer2
NR_122106.2:n.788del
NR_148704.1:n.1921del
NR_148705.1:n.1669del
XM_005264348.4:c.1141del	XP_005264405.1:p.Ser381HisfsTer2
XM_011532881.3:c.1069del	XP_011531183.1:p.Ser357HisfsTer2
XM_011532884.3:c.1141del	XP_011531186.1:p.Ser381HisfsTer2
XM_011532887.3:c.1141del	XP_011531189.1:p.Ser381HisfsTer2
XM_011532890.3:c.1141del	XP_011531192.1:p.Ser381HisfsTer2
XM_011532891.2:c.1069del	XP_011531193.1:p.Ser357HisfsTer2
XM_017004253.2:c.1141del	XP_016859742.1:p.Ser381HisfsTer2
XM_017004254.2:c.1141del	XP_016859743.1:p.Ser381HisfsTer2
XR_001738759.2:n.1603del
XR_001738760.2:n.1603del
XR_002959303.1:n.1603del
XR_244934.3:n.1603del
NM_015910.7:c.1141del MANE Select	NP_056994.3:p.Ser381HisfsTer2
NM_001354044.2:c.1069del	NP_001340973.1:p.Ser357HisfsTer2
NM_001354045.2:c.1141del	NP_001340974.1:p.Ser381HisfsTer2
NR_148704.2:n.1599del
NR_148705.2:n.1347del