Canonical Allele Identifier: CA1256317349
Gene: WDPCP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.63404356G= , CM000664.2:g.63404356G= GRCh38
NC_000002.11:g.63631491G= , CM000664.1:g.63631491G= GRCh37
NC_000002.10:g.63484995G= NCBI36
NG_028144.1:g.189377C=
NG_028144.2:g.441470C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272321.12:c.1127C= MANE Select ENSP00000272321.7:p.Thr376=
ENST00000272321.11:c.1127C= ENSP00000272321.7:p.Thr376=
ENST00000398544.7:c.650C= ENSP00000381552.3:p.Thr217=
ENST00000409120.5:c.551C= ENSP00000386769.1:p.Thr184=
ENST00000409199.5:c.551C= ENSP00000386592.1:p.Thr184=
ENST00000409354.6:c.488C= ENSP00000386795.2:p.Thr163=
ENST00000409562.7:c.1127C= ENSP00000387222.3:p.Thr376=
ENST00000409835.5:n.1374C=
ENST00000417238.5:c.*1238C= ENSP00000411429.1:n.*1238C=
ENST00000493315.1:n.829C=
NM_001042692.2:c.650C= NP_001036157.1:p.Thr217=
NM_015910.5:c.1127C= NP_056994.3:p.Thr376=
NR_122106.1:n.774C=
XM_005264348.2:c.1127C= XP_005264405.1:p.Thr376=
XM_011532881.1:c.1055C= XP_011531183.1:p.Thr352=
XM_011532882.1:c.1028C= XP_011531184.1:p.Thr343=
XM_011532883.1:c.1127C= XP_011531185.1:p.Thr376=
XM_011532884.1:c.1127C= XP_011531186.1:p.Thr376=
XM_011532885.1:c.1127C= XP_011531187.1:p.Thr376=
XM_011532886.1:c.1127C= XP_011531188.1:p.Thr376=
XM_011532887.1:c.1127C= XP_011531189.1:p.Thr376=
XM_011532888.1:c.1127C= XP_011531190.1:p.Thr376=
XM_011532889.1:c.1127C= XP_011531191.1:p.Thr376=
XM_011532890.1:c.1127C= XP_011531192.1:p.Thr376=
XM_011532891.1:c.1055C= XP_011531193.1:p.Thr352=
XR_244934.1:n.1374C=
XR_244935.1:n.1374C=
XR_939686.1:n.1374C=
NM_001042692.3:c.650C= NP_001036157.1:p.Thr217=
NM_001354044.1:c.1055C= NP_001340973.1:p.Thr352=
NM_001354045.1:c.1127C= NP_001340974.1:p.Thr376=
NM_015910.6:c.1127C= NP_056994.3:p.Thr376=
NR_122106.2:n.774C=
NR_148704.1:n.1907C=
NR_148705.1:n.1655C=
XM_005264348.4:c.1127C= XP_005264405.1:p.Thr376=
XM_011532881.3:c.1055C= XP_011531183.1:p.Thr352=
XM_011532884.3:c.1127C= XP_011531186.1:p.Thr376=
XM_011532887.3:c.1127C= XP_011531189.1:p.Thr376=
XM_011532890.3:c.1127C= XP_011531192.1:p.Thr376=
XM_011532891.2:c.1055C= XP_011531193.1:p.Thr352=
XM_017004253.2:c.1127C= XP_016859742.1:p.Thr376=
XM_017004254.2:c.1127C= XP_016859743.1:p.Thr376=
XR_001738759.2:n.1589C=
XR_001738760.2:n.1589C=
XR_002959303.1:n.1589C=
XR_244934.3:n.1589C=
NM_015910.7:c.1127C= MANE Select NP_056994.3:p.Thr376=
NM_001354044.2:c.1055C= NP_001340973.1:p.Thr352=
NM_001354045.2:c.1127C= NP_001340974.1:p.Thr376=
NR_148704.2:n.1585C=
NR_148705.2:n.1333C=