Canonical Allele Identifier: CA347056445

Gene: WDPCP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.63174697T>C , CM000664.2:g.63174697T>C	GRCh38
NC_000002.11:g.63401832T>C , CM000664.1:g.63401832T>C	GRCh37
NC_000002.10:g.63255336T>C	NCBI36
NG_028144.1:g.419036A>G
NG_028144.2:g.671129A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015910.7:c.2051A>G MANE Select	NP_056994.3:p.Gln684Arg
ENST00000272321.12:c.2051A>G MANE Select	ENSP00000272321.7:p.Gln684Arg
NM_001042692.2:c.1574A>G	NP_001036157.1:p.Gln525Arg
NM_001042692.3:c.1574A>G	NP_001036157.1:p.Gln525Arg
NM_001354044.1:c.1979A>G	NP_001340973.1:p.Gln660Arg
NM_001354044.2:c.1979A>G	NP_001340973.1:p.Gln660Arg
NM_015910.5:c.2051A>G	NP_056994.3:p.Gln684Arg
NM_015910.6:c.2051A>G	NP_056994.3:p.Gln684Arg
NR_122106.1:n.1694A>G
NR_122106.2:n.1694A>G
NR_148704.1:n.2827A>G
NR_148704.2:n.2505A>G
NR_148705.1:n.2476A>G
NR_148705.2:n.2154A>G
ENST00000272321.11:c.2051A>G	ENSP00000272321.7:p.Gln684Arg
ENST00000398544.7:c.1574A>G	ENSP00000381552.3:p.Gln525Arg
ENST00000409120.5:c.1475A>G	ENSP00000386769.1:p.Gln492Arg
ENST00000409199.5:c.1475A>G	ENSP00000386592.1:p.Gln492Arg
ENST00000409354.6:c.1309A>G	ENSP00000386795.2:n.1309A>G
XM_005264348.2:c.2051A>G	XP_005264405.1:p.Gln684Arg
XM_005264348.4:c.2051A>G	XP_005264405.1:p.Gln684Arg
XM_011532881.1:c.1979A>G	XP_011531183.1:p.Gln660Arg
XM_011532881.3:c.1979A>G	XP_011531183.1:p.Gln660Arg
XM_011532882.1:c.1952A>G	XP_011531184.1:p.Gln651Arg
XM_011532883.1:c.2051A>G	XP_011531185.1:p.Gln684Arg
XR_001738759.2:n.2410A>G
XR_001738760.2:n.2508A>G
XR_002959303.1:n.2747A>G
XR_244934.1:n.2294A>G
XR_244934.3:n.2509A>G
XR_244935.1:n.2195A>G