Canonical Allele Identifier: CA1256317328

Gene: WDPCP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.63404289T= , CM000664.2:g.63404289T=	GRCh38
NC_000002.11:g.63631424T= , CM000664.1:g.63631424T=	GRCh37
NC_000002.10:g.63484928T=	NCBI36
NG_028144.1:g.189444A=
NG_028144.2:g.441537A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272321.12:c.1194A= MANE Select	ENSP00000272321.7:p.Gln398=
ENST00000272321.11:c.1194A=	ENSP00000272321.7:p.Gln398=
ENST00000398544.7:c.717A=	ENSP00000381552.3:p.Gln239=
ENST00000409120.5:c.618A=	ENSP00000386769.1:p.Gln206=
ENST00000409199.5:c.618A=	ENSP00000386592.1:p.Gln206=
ENST00000409354.6:c.555A=	ENSP00000386795.2:p.Gln185=
ENST00000409562.7:c.1194A=	ENSP00000387222.3:p.Gln398=
ENST00000409835.5:n.1441A=
ENST00000417238.5:c.*1305A=	ENSP00000411429.1:n.*1305A=
ENST00000493315.1:n.896A=
NM_001042692.2:c.717A=	NP_001036157.1:p.Gln239=
NM_015910.5:c.1194A=	NP_056994.3:p.Gln398=
NR_122106.1:n.841A=
XM_005264348.2:c.1194A=	XP_005264405.1:p.Gln398=
XM_011532881.1:c.1122A=	XP_011531183.1:p.Gln374=
XM_011532882.1:c.1095A=	XP_011531184.1:p.Gln365=
XM_011532883.1:c.1194A=	XP_011531185.1:p.Gln398=
XM_011532884.1:c.1194A=	XP_011531186.1:p.Gln398=
XM_011532885.1:c.1194A=	XP_011531187.1:p.Gln398=
XM_011532886.1:c.1194A=	XP_011531188.1:p.Gln398=
XM_011532887.1:c.1194A=	XP_011531189.1:p.Gln398=
XM_011532888.1:c.1194A=	XP_011531190.1:p.Gln398=
XM_011532889.1:c.1194A=	XP_011531191.1:p.Gln398=
XM_011532890.1:c.1194A=	XP_011531192.1:p.Gln398=
XM_011532891.1:c.1122A=	XP_011531193.1:p.Gln374=
XR_244934.1:n.1441A=
XR_244935.1:n.1441A=
XR_939686.1:n.1441A=
NM_001042692.3:c.717A=	NP_001036157.1:p.Gln239=
NM_001354044.1:c.1122A=	NP_001340973.1:p.Gln374=
NM_001354045.1:c.1194A=	NP_001340974.1:p.Gln398=
NM_015910.6:c.1194A=	NP_056994.3:p.Gln398=
NR_122106.2:n.841A=
NR_148704.1:n.1974A=
NR_148705.1:n.1722A=
XM_005264348.4:c.1194A=	XP_005264405.1:p.Gln398=
XM_011532881.3:c.1122A=	XP_011531183.1:p.Gln374=
XM_011532884.3:c.1194A=	XP_011531186.1:p.Gln398=
XM_011532887.3:c.1194A=	XP_011531189.1:p.Gln398=
XM_011532890.3:c.1194A=	XP_011531192.1:p.Gln398=
XM_011532891.2:c.1122A=	XP_011531193.1:p.Gln374=
XM_017004253.2:c.1194A=	XP_016859742.1:p.Gln398=
XM_017004254.2:c.1194A=	XP_016859743.1:p.Gln398=
XR_001738759.2:n.1656A=
XR_001738760.2:n.1656A=
XR_002959303.1:n.1656A=
XR_244934.3:n.1656A=
NM_015910.7:c.1194A= MANE Select	NP_056994.3:p.Gln398=
NM_001354044.2:c.1122A=	NP_001340973.1:p.Gln374=
NM_001354045.2:c.1194A=	NP_001340974.1:p.Gln398=
NR_148704.2:n.1652A=
NR_148705.2:n.1400A=