Canonical Allele Identifier: CA347065257

Gene: WDPCP

Linked Data

• MyVariant Identifiers: chr2:g.63631573C>A (hg19) ; chr2:g.63404438C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.63404438C>A , CM000664.2:g.63404438C>A	GRCh38
NC_000002.11:g.63631573C>A , CM000664.1:g.63631573C>A	GRCh37
NC_000002.10:g.63485077C>A	NCBI36
NG_028144.1:g.189295G>T
NG_028144.2:g.441388G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272321.12:c.1045G>T MANE Select	ENSP00000272321.7:p.Glu349Ter
ENST00000272321.11:c.1045G>T	ENSP00000272321.7:p.Glu349Ter
ENST00000398544.7:c.568G>T	ENSP00000381552.3:p.Glu190Ter
ENST00000409120.5:c.469G>T	ENSP00000386769.1:p.Glu157Ter
ENST00000409199.5:c.469G>T	ENSP00000386592.1:p.Glu157Ter
ENST00000409354.6:c.406G>T	ENSP00000386795.2:p.Glu136Ter
ENST00000409562.7:c.1045G>T	ENSP00000387222.3:p.Glu349Ter
ENST00000409835.5:n.1292G>T
ENST00000417238.5:c.*1156G>T	ENSP00000411429.1:n.*1156G>T
ENST00000493315.1:n.747G>T
NM_001042692.2:c.568G>T	NP_001036157.1:p.Glu190Ter
NM_015910.5:c.1045G>T	NP_056994.3:p.Glu349Ter
NR_122106.1:n.692G>T
XM_005264348.2:c.1045G>T	XP_005264405.1:p.Glu349Ter
XM_011532881.1:c.973G>T	XP_011531183.1:p.Glu325Ter
XM_011532882.1:c.946G>T	XP_011531184.1:p.Glu316Ter
XM_011532883.1:c.1045G>T	XP_011531185.1:p.Glu349Ter
XM_011532884.1:c.1045G>T	XP_011531186.1:p.Glu349Ter
XM_011532885.1:c.1045G>T	XP_011531187.1:p.Glu349Ter
XM_011532886.1:c.1045G>T	XP_011531188.1:p.Glu349Ter
XM_011532887.1:c.1045G>T	XP_011531189.1:p.Glu349Ter
XM_011532888.1:c.1045G>T	XP_011531190.1:p.Glu349Ter
XM_011532889.1:c.1045G>T	XP_011531191.1:p.Glu349Ter
XM_011532890.1:c.1045G>T	XP_011531192.1:p.Glu349Ter
XM_011532891.1:c.973G>T	XP_011531193.1:p.Glu325Ter
XR_244934.1:n.1292G>T
XR_244935.1:n.1292G>T
XR_939686.1:n.1292G>T
NM_001042692.3:c.568G>T	NP_001036157.1:p.Glu190Ter
NM_001354044.1:c.973G>T	NP_001340973.1:p.Glu325Ter
NM_001354045.1:c.1045G>T	NP_001340974.1:p.Glu349Ter
NM_015910.6:c.1045G>T	NP_056994.3:p.Glu349Ter
NR_122106.2:n.692G>T
NR_148704.1:n.1825G>T
NR_148705.1:n.1573G>T
XM_005264348.4:c.1045G>T	XP_005264405.1:p.Glu349Ter
XM_011532881.3:c.973G>T	XP_011531183.1:p.Glu325Ter
XM_011532884.3:c.1045G>T	XP_011531186.1:p.Glu349Ter
XM_011532887.3:c.1045G>T	XP_011531189.1:p.Glu349Ter
XM_011532890.3:c.1045G>T	XP_011531192.1:p.Glu349Ter
XM_011532891.2:c.973G>T	XP_011531193.1:p.Glu325Ter
XM_017004253.2:c.1045G>T	XP_016859742.1:p.Glu349Ter
XM_017004254.2:c.1045G>T	XP_016859743.1:p.Glu349Ter
XR_001738759.2:n.1507G>T
XR_001738760.2:n.1507G>T
XR_002959303.1:n.1507G>T
XR_244934.3:n.1507G>T
NM_015910.7:c.1045G>T MANE Select	NP_056994.3:p.Glu349Ter
NM_001354044.2:c.973G>T	NP_001340973.1:p.Glu325Ter
NM_001354045.2:c.1045G>T	NP_001340974.1:p.Glu349Ter
NR_148704.2:n.1503G>T
NR_148705.2:n.1251G>T