Canonical Allele Identifier: CA1256317406

Gene: WDPCP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.63404487G= , CM000664.2:g.63404487G=	GRCh38
NC_000002.11:g.63631622G= , CM000664.1:g.63631622G=	GRCh37
NC_000002.10:g.63485126G=	NCBI36
NG_028144.1:g.189246C=
NG_028144.2:g.441339C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272321.12:c.996C= MANE Select	ENSP00000272321.7:p.Thr332=
ENST00000272321.11:c.996C=	ENSP00000272321.7:p.Thr332=
ENST00000398544.7:c.519C=	ENSP00000381552.3:p.Thr173=
ENST00000409120.5:c.420C=	ENSP00000386769.1:p.Thr140=
ENST00000409199.5:c.420C=	ENSP00000386592.1:p.Thr140=
ENST00000409354.6:c.357C=	ENSP00000386795.2:p.Thr119=
ENST00000409562.7:c.996C=	ENSP00000387222.3:p.Thr332=
ENST00000409835.5:n.1243C=
ENST00000417238.5:c.*1107C=	ENSP00000411429.1:n.*1107C=
ENST00000493315.1:n.698C=
NM_001042692.2:c.519C=	NP_001036157.1:p.Thr173=
NM_015910.5:c.996C=	NP_056994.3:p.Thr332=
NR_122106.1:n.643C=
XM_005264348.2:c.996C=	XP_005264405.1:p.Thr332=
XM_011532881.1:c.924C=	XP_011531183.1:p.Thr308=
XM_011532882.1:c.897C=	XP_011531184.1:p.Thr299=
XM_011532883.1:c.996C=	XP_011531185.1:p.Thr332=
XM_011532884.1:c.996C=	XP_011531186.1:p.Thr332=
XM_011532885.1:c.996C=	XP_011531187.1:p.Thr332=
XM_011532886.1:c.996C=	XP_011531188.1:p.Thr332=
XM_011532887.1:c.996C=	XP_011531189.1:p.Thr332=
XM_011532888.1:c.996C=	XP_011531190.1:p.Thr332=
XM_011532889.1:c.996C=	XP_011531191.1:p.Thr332=
XM_011532890.1:c.996C=	XP_011531192.1:p.Thr332=
XM_011532891.1:c.924C=	XP_011531193.1:p.Thr308=
XR_244934.1:n.1243C=
XR_244935.1:n.1243C=
XR_939686.1:n.1243C=
NM_001042692.3:c.519C=	NP_001036157.1:p.Thr173=
NM_001354044.1:c.924C=	NP_001340973.1:p.Thr308=
NM_001354045.1:c.996C=	NP_001340974.1:p.Thr332=
NM_015910.6:c.996C=	NP_056994.3:p.Thr332=
NR_122106.2:n.643C=
NR_148704.1:n.1776C=
NR_148705.1:n.1524C=
XM_005264348.4:c.996C=	XP_005264405.1:p.Thr332=
XM_011532881.3:c.924C=	XP_011531183.1:p.Thr308=
XM_011532884.3:c.996C=	XP_011531186.1:p.Thr332=
XM_011532887.3:c.996C=	XP_011531189.1:p.Thr332=
XM_011532890.3:c.996C=	XP_011531192.1:p.Thr332=
XM_011532891.2:c.924C=	XP_011531193.1:p.Thr308=
XM_017004253.2:c.996C=	XP_016859742.1:p.Thr332=
XM_017004254.2:c.996C=	XP_016859743.1:p.Thr332=
XR_001738759.2:n.1458C=
XR_001738760.2:n.1458C=
XR_002959303.1:n.1458C=
XR_244934.3:n.1458C=
NM_015910.7:c.996C= MANE Select	NP_056994.3:p.Thr332=
NM_001354044.2:c.924C=	NP_001340973.1:p.Thr308=
NM_001354045.2:c.996C=	NP_001340974.1:p.Thr332=
NR_148704.2:n.1454C=
NR_148705.2:n.1202C=