Canonical Allele Identifier: CA347065353

Gene: WDPCP

Linked Data

• MyVariant Identifiers: chr2:g.63631617A>C (hg19) ; chr2:g.63404482A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.63404482A>C , CM000664.2:g.63404482A>C	GRCh38
NC_000002.11:g.63631617A>C , CM000664.1:g.63631617A>C	GRCh37
NC_000002.10:g.63485121A>C	NCBI36
NG_028144.1:g.189251T>G
NG_028144.2:g.441344T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272321.12:c.1001T>G MANE Select	ENSP00000272321.7:p.Ile334Arg
ENST00000272321.11:c.1001T>G	ENSP00000272321.7:p.Ile334Arg
ENST00000398544.7:c.524T>G	ENSP00000381552.3:p.Ile175Arg
ENST00000409120.5:c.425T>G	ENSP00000386769.1:p.Ile142Arg
ENST00000409199.5:c.425T>G	ENSP00000386592.1:p.Ile142Arg
ENST00000409354.6:c.362T>G	ENSP00000386795.2:p.Ile121Arg
ENST00000409562.7:c.1001T>G	ENSP00000387222.3:p.Ile334Arg
ENST00000409835.5:n.1248T>G
ENST00000417238.5:c.*1112T>G	ENSP00000411429.1:n.*1112T>G
ENST00000493315.1:n.703T>G
NM_001042692.2:c.524T>G	NP_001036157.1:p.Ile175Arg
NM_015910.5:c.1001T>G	NP_056994.3:p.Ile334Arg
NR_122106.1:n.648T>G
XM_005264348.2:c.1001T>G	XP_005264405.1:p.Ile334Arg
XM_011532881.1:c.929T>G	XP_011531183.1:p.Ile310Arg
XM_011532882.1:c.902T>G	XP_011531184.1:p.Ile301Arg
XM_011532883.1:c.1001T>G	XP_011531185.1:p.Ile334Arg
XM_011532884.1:c.1001T>G	XP_011531186.1:p.Ile334Arg
XM_011532885.1:c.1001T>G	XP_011531187.1:p.Ile334Arg
XM_011532886.1:c.1001T>G	XP_011531188.1:p.Ile334Arg
XM_011532887.1:c.1001T>G	XP_011531189.1:p.Ile334Arg
XM_011532888.1:c.1001T>G	XP_011531190.1:p.Ile334Arg
XM_011532889.1:c.1001T>G	XP_011531191.1:p.Ile334Arg
XM_011532890.1:c.1001T>G	XP_011531192.1:p.Ile334Arg
XM_011532891.1:c.929T>G	XP_011531193.1:p.Ile310Arg
XR_244934.1:n.1248T>G
XR_244935.1:n.1248T>G
XR_939686.1:n.1248T>G
NM_001042692.3:c.524T>G	NP_001036157.1:p.Ile175Arg
NM_001354044.1:c.929T>G	NP_001340973.1:p.Ile310Arg
NM_001354045.1:c.1001T>G	NP_001340974.1:p.Ile334Arg
NM_015910.6:c.1001T>G	NP_056994.3:p.Ile334Arg
NR_122106.2:n.648T>G
NR_148704.1:n.1781T>G
NR_148705.1:n.1529T>G
XM_005264348.4:c.1001T>G	XP_005264405.1:p.Ile334Arg
XM_011532881.3:c.929T>G	XP_011531183.1:p.Ile310Arg
XM_011532884.3:c.1001T>G	XP_011531186.1:p.Ile334Arg
XM_011532887.3:c.1001T>G	XP_011531189.1:p.Ile334Arg
XM_011532890.3:c.1001T>G	XP_011531192.1:p.Ile334Arg
XM_011532891.2:c.929T>G	XP_011531193.1:p.Ile310Arg
XM_017004253.2:c.1001T>G	XP_016859742.1:p.Ile334Arg
XM_017004254.2:c.1001T>G	XP_016859743.1:p.Ile334Arg
XR_001738759.2:n.1463T>G
XR_001738760.2:n.1463T>G
XR_002959303.1:n.1463T>G
XR_244934.3:n.1463T>G
NM_015910.7:c.1001T>G MANE Select	NP_056994.3:p.Ile334Arg
NM_001354044.2:c.929T>G	NP_001340973.1:p.Ile310Arg
NM_001354045.2:c.1001T>G	NP_001340974.1:p.Ile334Arg
NR_148704.2:n.1459T>G
NR_148705.2:n.1207T>G