Canonical Allele Identifier: CA10613776

Gene: WDPCP

Linked Data

• ClinVar Variation Id: 336748
• ClinVar RCV Id: RCV000287152
• dbSNP Id: rs886056219
• gnomAD v2: 2-63348535-TTG-T
• gnomAD v3: 2-63121400-TTG-T
• gnomAD v4: 2-63121400-TTG-T
• MyVariant Identifiers: chr2:g.63348536_63348537del (hg19) ; chr2:g.63121401_63121402del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.63121401_63121402del , CM000664.2:g.63121401_63121402del	GRCh38
NC_000002.11:g.63348536_63348537del , CM000664.1:g.63348536_63348537del	GRCh37
NC_000002.10:g.63202040_63202041del	NCBI36
NG_028144.1:g.472331_472332del
NG_028144.2:g.724424_724425del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272321.12:c.*604_*605del MANE Select	ENSP00000272321.7:n.*604_*605del
ENST00000272321.11:c.*604_*605del	ENSP00000272321.7:n.*604_*605del
ENST00000409354.6:c.2103_2104del	ENSP00000386795.2:n.2103_2104del
NM_001042692.2:c.*604_*605del	NP_001036157.1:n.*604_*605del
NM_015910.5:c.*604_*605del	NP_056994.3:n.*604_*605del
NR_122106.1:n.2488_2489del
XM_005264348.2:c.*419_*420del	XP_005264405.1:n.*419_*420del
XM_011532881.1:c.*419_*420del	XP_011531183.1:n.*419_*420del
XM_011532882.1:c.*419_*420del	XP_011531184.1:n.*419_*420del
NM_001042692.3:c.*604_*605del	NP_001036157.1:n.*604_*605del
NM_001354044.1:c.*604_*605del	NP_001340973.1:n.*604_*605del
NM_015910.6:c.*604_*605del	NP_056994.3:n.*604_*605del
NR_122106.2:n.2488_2489del
NR_148704.1:n.3621_3622del
NR_148705.1:n.3270_3271del
XM_005264348.4:c.*419_*420del	XP_005264405.1:n.*419_*420del
XM_011532881.3:c.*419_*420del	XP_011531183.1:n.*419_*420del
XR_244934.3:n.3303_3304del
NM_015910.7:c.*604_*605del MANE Select	NP_056994.3:n.*604_*605del
NM_001354044.2:c.*604_*605del	NP_001340973.1:n.*604_*605del
NR_148704.2:n.3299_3300del
NR_148705.2:n.2948_2949del