Canonical Allele Identifier: CA347065326

Gene: WDPCP

Linked Data

• MyVariant Identifiers: chr2:g.63631605G>A (hg19) ; chr2:g.63404470G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.63404470G>A , CM000664.2:g.63404470G>A	GRCh38
NC_000002.11:g.63631605G>A , CM000664.1:g.63631605G>A	GRCh37
NC_000002.10:g.63485109G>A	NCBI36
NG_028144.1:g.189263C>T
NG_028144.2:g.441356C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272321.12:c.1013C>T MANE Select	ENSP00000272321.7:p.Ser338Leu
ENST00000272321.11:c.1013C>T	ENSP00000272321.7:p.Ser338Leu
ENST00000398544.7:c.536C>T	ENSP00000381552.3:p.Ser179Leu
ENST00000409120.5:c.437C>T	ENSP00000386769.1:p.Ser146Leu
ENST00000409199.5:c.437C>T	ENSP00000386592.1:p.Ser146Leu
ENST00000409354.6:c.374C>T	ENSP00000386795.2:p.Ser125Leu
ENST00000409562.7:c.1013C>T	ENSP00000387222.3:p.Ser338Leu
ENST00000409835.5:n.1260C>T
ENST00000417238.5:c.*1124C>T	ENSP00000411429.1:n.*1124C>T
ENST00000493315.1:n.715C>T
NM_001042692.2:c.536C>T	NP_001036157.1:p.Ser179Leu
NM_015910.5:c.1013C>T	NP_056994.3:p.Ser338Leu
NR_122106.1:n.660C>T
XM_005264348.2:c.1013C>T	XP_005264405.1:p.Ser338Leu
XM_011532881.1:c.941C>T	XP_011531183.1:p.Ser314Leu
XM_011532882.1:c.914C>T	XP_011531184.1:p.Ser305Leu
XM_011532883.1:c.1013C>T	XP_011531185.1:p.Ser338Leu
XM_011532884.1:c.1013C>T	XP_011531186.1:p.Ser338Leu
XM_011532885.1:c.1013C>T	XP_011531187.1:p.Ser338Leu
XM_011532886.1:c.1013C>T	XP_011531188.1:p.Ser338Leu
XM_011532887.1:c.1013C>T	XP_011531189.1:p.Ser338Leu
XM_011532888.1:c.1013C>T	XP_011531190.1:p.Ser338Leu
XM_011532889.1:c.1013C>T	XP_011531191.1:p.Ser338Leu
XM_011532890.1:c.1013C>T	XP_011531192.1:p.Ser338Leu
XM_011532891.1:c.941C>T	XP_011531193.1:p.Ser314Leu
XR_244934.1:n.1260C>T
XR_244935.1:n.1260C>T
XR_939686.1:n.1260C>T
NM_001042692.3:c.536C>T	NP_001036157.1:p.Ser179Leu
NM_001354044.1:c.941C>T	NP_001340973.1:p.Ser314Leu
NM_001354045.1:c.1013C>T	NP_001340974.1:p.Ser338Leu
NM_015910.6:c.1013C>T	NP_056994.3:p.Ser338Leu
NR_122106.2:n.660C>T
NR_148704.1:n.1793C>T
NR_148705.1:n.1541C>T
XM_005264348.4:c.1013C>T	XP_005264405.1:p.Ser338Leu
XM_011532881.3:c.941C>T	XP_011531183.1:p.Ser314Leu
XM_011532884.3:c.1013C>T	XP_011531186.1:p.Ser338Leu
XM_011532887.3:c.1013C>T	XP_011531189.1:p.Ser338Leu
XM_011532890.3:c.1013C>T	XP_011531192.1:p.Ser338Leu
XM_011532891.2:c.941C>T	XP_011531193.1:p.Ser314Leu
XM_017004253.2:c.1013C>T	XP_016859742.1:p.Ser338Leu
XM_017004254.2:c.1013C>T	XP_016859743.1:p.Ser338Leu
XR_001738759.2:n.1475C>T
XR_001738760.2:n.1475C>T
XR_002959303.1:n.1475C>T
XR_244934.3:n.1475C>T
NM_015910.7:c.1013C>T MANE Select	NP_056994.3:p.Ser338Leu
NM_001354044.2:c.941C>T	NP_001340973.1:p.Ser314Leu
NM_001354045.2:c.1013C>T	NP_001340974.1:p.Ser338Leu
NR_148704.2:n.1471C>T
NR_148705.2:n.1219C>T