Canonical Allele Identifier: CA1256317378

Gene: WDPCP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.63404411C= , CM000664.2:g.63404411C=	GRCh38
NC_000002.11:g.63631546C= , CM000664.1:g.63631546C=	GRCh37
NC_000002.10:g.63485050C=	NCBI36
NG_028144.1:g.189322G=
NG_028144.2:g.441415G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272321.12:c.1072G= MANE Select	ENSP00000272321.7:p.Asp358=
ENST00000272321.11:c.1072G=	ENSP00000272321.7:p.Asp358=
ENST00000398544.7:c.595G=	ENSP00000381552.3:p.Asp199=
ENST00000409120.5:c.496G=	ENSP00000386769.1:p.Asp166=
ENST00000409199.5:c.496G=	ENSP00000386592.1:p.Asp166=
ENST00000409354.6:c.433G=	ENSP00000386795.2:p.Asp145=
ENST00000409562.7:c.1072G=	ENSP00000387222.3:p.Asp358=
ENST00000409835.5:n.1319G=
ENST00000417238.5:c.*1183G=	ENSP00000411429.1:n.*1183G=
ENST00000493315.1:n.774G=
NM_001042692.2:c.595G=	NP_001036157.1:p.Asp199=
NM_015910.5:c.1072G=	NP_056994.3:p.Asp358=
NR_122106.1:n.719G=
XM_005264348.2:c.1072G=	XP_005264405.1:p.Asp358=
XM_011532881.1:c.1000G=	XP_011531183.1:p.Asp334=
XM_011532882.1:c.973G=	XP_011531184.1:p.Asp325=
XM_011532883.1:c.1072G=	XP_011531185.1:p.Asp358=
XM_011532884.1:c.1072G=	XP_011531186.1:p.Asp358=
XM_011532885.1:c.1072G=	XP_011531187.1:p.Asp358=
XM_011532886.1:c.1072G=	XP_011531188.1:p.Asp358=
XM_011532887.1:c.1072G=	XP_011531189.1:p.Asp358=
XM_011532888.1:c.1072G=	XP_011531190.1:p.Asp358=
XM_011532889.1:c.1072G=	XP_011531191.1:p.Asp358=
XM_011532890.1:c.1072G=	XP_011531192.1:p.Asp358=
XM_011532891.1:c.1000G=	XP_011531193.1:p.Asp334=
XR_244934.1:n.1319G=
XR_244935.1:n.1319G=
XR_939686.1:n.1319G=
NM_001042692.3:c.595G=	NP_001036157.1:p.Asp199=
NM_001354044.1:c.1000G=	NP_001340973.1:p.Asp334=
NM_001354045.1:c.1072G=	NP_001340974.1:p.Asp358=
NM_015910.6:c.1072G=	NP_056994.3:p.Asp358=
NR_122106.2:n.719G=
NR_148704.1:n.1852G=
NR_148705.1:n.1600G=
XM_005264348.4:c.1072G=	XP_005264405.1:p.Asp358=
XM_011532881.3:c.1000G=	XP_011531183.1:p.Asp334=
XM_011532884.3:c.1072G=	XP_011531186.1:p.Asp358=
XM_011532887.3:c.1072G=	XP_011531189.1:p.Asp358=
XM_011532890.3:c.1072G=	XP_011531192.1:p.Asp358=
XM_011532891.2:c.1000G=	XP_011531193.1:p.Asp334=
XM_017004253.2:c.1072G=	XP_016859742.1:p.Asp358=
XM_017004254.2:c.1072G=	XP_016859743.1:p.Asp358=
XR_001738759.2:n.1534G=
XR_001738760.2:n.1534G=
XR_002959303.1:n.1534G=
XR_244934.3:n.1534G=
NM_015910.7:c.1072G= MANE Select	NP_056994.3:p.Asp358=
NM_001354044.2:c.1000G=	NP_001340973.1:p.Asp334=
NM_001354045.2:c.1072G=	NP_001340974.1:p.Asp358=
NR_148704.2:n.1530G=
NR_148705.2:n.1278G=