Canonical Allele Identifier: CA170897

Gene: CRPPA CRPPA-AS1

Linked Data

• ClinVar Variation Id: 156455
• ClinVar RCV Id: RCV000144516 ; RCV000596292 ; RCV000714703 ; RCV002228673
• dbSNP Id: rs587777798
• ExAC: 7:16298017 AAAC / A
• gnomAD v2: 7-16298017-AAAC-A
• gnomAD v3: 7-16258392-AAAC-A
• gnomAD v4: 7-16258392-AAAC-A
• MyVariant Identifiers: chr7:g.16298018_16298020del (hg19) ; chr7:g.16258393_16258395del (hg38)
• PubMed: PMID:23390185

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.16258403_16258405del , CM000669.2:g.16258403_16258405del	GRCh38
NC_000007.13:g.16298028_16298030del , CM000669.1:g.16298028_16298030del	GRCh37
NC_000007.12:g.16264553_16264555del	NCBI36
NG_032690.1:g.167928_167930del
NG_032690.2:g.167928_167930del

Transcript Alleles

HGVS	Amino-acid change
ENST00000407010.7:c.1114_1116del (CRPPA) MANE Select	ENSP00000385478.2:p.Val372del
ENST00000674759.1:c.811_813del (CRPPA)	ENSP00000502749.1:p.Val271del
ENST00000675257.1:c.706_708del (CRPPA)	ENSP00000501664.1:p.Val236del
ENST00000676325.1:c.811_813del (CRPPA)	ENSP00000502074.1:p.Val271del
ENST00000399310.3:c.964_966del (CRPPA)	ENSP00000382249.3:p.Val322del
ENST00000407010.6:c.1114_1116del (CRPPA)	ENSP00000385478.2:p.Val372del
NM_001101417.3:c.964_966del (CRPPA)	NP_001094887.1:p.Val322del
NM_001101426.3:c.1114_1116del (CRPPA)	NP_001094896.1:p.Val372del
NR_038946.1:n.224-3496_224-3494del (CRPPA-AS1)
NR_038947.1:n.241-7824_241-7822del (CRPPA-AS1)
XM_006715770.2:c.865_867del (CRPPA)	XP_006715833.1:p.Val289del
XM_011515497.1:c.1114_1116del (CRPPA)	XP_011513799.1:p.Val372del
XM_011515498.1:c.1114_1116del (CRPPA)	XP_011513800.1:p.Val372del
XM_011515499.1:c.1114_1116del (CRPPA)	XP_011513801.1:p.Val372del
XM_011515500.1:c.1009_1011del (CRPPA)	XP_011513802.1:p.Val337del
XM_011515502.1:c.811_813del (CRPPA)	XP_011513804.1:p.Val271del
XM_011515503.1:c.811_813del (CRPPA)	XP_011513805.1:p.Val271del
XM_011515504.1:c.811_813del (CRPPA)	XP_011513806.1:p.Val271del
XM_011515505.1:c.811_813del (CRPPA)	XP_011513807.1:p.Val271del
XM_011515506.1:c.811_813del (CRPPA)	XP_011513808.1:p.Val271del
XM_011515507.1:c.811_813del (CRPPA)	XP_011513809.1:p.Val271del
XM_011515508.1:c.811_813del (CRPPA)	XP_011513810.1:p.Val271del
XM_011515509.1:c.811_813del (CRPPA)	XP_011513811.1:p.Val271del
XM_006715770.3:c.865_867del (CRPPA)	XP_006715833.1:p.Val289del
XM_011515499.2:c.1114_1116del (CRPPA)	XP_011513801.1:p.Val372del
XM_011515500.2:c.1009_1011del (CRPPA)	XP_011513802.1:p.Val337del
XM_011515508.2:c.811_813del (CRPPA)	XP_011513810.1:p.Val271del
XM_011515509.2:c.811_813del (CRPPA)	XP_011513811.1:p.Val271del
XM_017012575.1:c.1114_1116del (CRPPA)	XP_016868064.1:p.Val372del
XM_017012577.1:c.478_480del (CRPPA)	XP_016868066.1:p.Val160del
XM_017012578.1:c.478_480del (CRPPA)	XP_016868067.1:p.Val160del
XM_024446909.1:c.811_813del (CRPPA)	XP_024302677.1:p.Val271del
XM_024446910.1:c.811_813del (CRPPA)	XP_024302678.1:p.Val271del
XM_024446911.1:c.706_708del (CRPPA)	XP_024302679.1:p.Val236del
XR_001744866.1:n.1355_1357del (CRPPA)
XR_001744868.1:n.1122_1124del (CRPPA)
NM_001101426.4:c.1114_1116del (CRPPA) MANE Select	NP_001094896.1:p.Val372del
NM_001101417.4:c.964_966del (CRPPA)	NP_001094887.1:p.Val322del
NM_001368197.1:c.1009_1011del (CRPPA)	NP_001355126.1:p.Val337del
NR_160656.1:n.1179_1181del (CRPPA)