Canonical Allele Identifier: CA2518460426
Gene: CRPPA HGNC NCBI
CRPPA-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1950314
ClinVar RCV Id: RCV002671693
gnomAD v4: 7-16259016-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.16259016G>T , CM000669.2:g.16259016G>T GRCh38
NC_000007.13:g.16298641G>T , CM000669.1:g.16298641G>T GRCh37
NC_000007.12:g.16265166G>T NCBI36
NG_032690.1:g.167307C>A
NG_032690.2:g.167307C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000407010.7:c.934-4C>A (CRPPA) MANE Select ENSP00000385478.2:n.934-4C>A
ENST00000674759.1:c.631-4C>A (CRPPA) ENSP00000502749.1:n.631-4C>A
ENST00000675257.1:c.526-4C>A (CRPPA) ENSP00000501664.1:n.526-4C>A
ENST00000676325.1:c.631-4C>A (CRPPA) ENSP00000502074.1:n.631-4C>A
ENST00000399310.3:c.784-4C>A (CRPPA) ENSP00000382249.3:n.784-4C>A
ENST00000407010.6:c.934-4C>A (CRPPA) ENSP00000385478.2:n.934-4C>A
NM_001101417.3:c.784-4C>A (CRPPA) NP_001094887.1:n.784-4C>A
NM_001101426.3:c.934-4C>A (CRPPA) NP_001094896.1:n.934-4C>A
NR_038946.1:n.224-2883G>T (CRPPA-AS1)
NR_038947.1:n.241-7211G>T (CRPPA-AS1)
XM_006715770.2:c.685-4C>A (CRPPA) XP_006715833.1:n.685-4C>A
XM_011515497.1:c.934-4C>A (CRPPA) XP_011513799.1:n.934-4C>A
XM_011515498.1:c.934-4C>A (CRPPA) XP_011513800.1:n.934-4C>A
XM_011515499.1:c.934-4C>A (CRPPA) XP_011513801.1:n.934-4C>A
XM_011515500.1:c.829-4C>A (CRPPA) XP_011513802.1:n.829-4C>A
XM_011515502.1:c.631-4C>A (CRPPA) XP_011513804.1:n.631-4C>A
XM_011515503.1:c.631-4C>A (CRPPA) XP_011513805.1:n.631-4C>A
XM_011515504.1:c.631-4C>A (CRPPA) XP_011513806.1:n.631-4C>A
XM_011515505.1:c.631-4C>A (CRPPA) XP_011513807.1:n.631-4C>A
XM_011515506.1:c.631-4C>A (CRPPA) XP_011513808.1:n.631-4C>A
XM_011515507.1:c.631-4C>A (CRPPA) XP_011513809.1:n.631-4C>A
XM_011515508.1:c.631-4C>A (CRPPA) XP_011513810.1:n.631-4C>A
XM_011515509.1:c.631-4C>A (CRPPA) XP_011513811.1:n.631-4C>A
XM_006715770.3:c.685-4C>A (CRPPA) XP_006715833.1:n.685-4C>A
XM_011515499.2:c.934-4C>A (CRPPA) XP_011513801.1:n.934-4C>A
XM_011515500.2:c.829-4C>A (CRPPA) XP_011513802.1:n.829-4C>A
XM_011515508.2:c.631-4C>A (CRPPA) XP_011513810.1:n.631-4C>A
XM_011515509.2:c.631-4C>A (CRPPA) XP_011513811.1:n.631-4C>A
XM_017012575.1:c.934-4C>A (CRPPA) XP_016868064.1:n.934-4C>A
XM_017012577.1:c.298-4C>A (CRPPA) XP_016868066.1:n.298-4C>A
XM_017012578.1:c.298-4C>A (CRPPA) XP_016868067.1:n.298-4C>A
XM_024446909.1:c.631-4C>A (CRPPA) XP_024302677.1:n.631-4C>A
XM_024446910.1:c.631-4C>A (CRPPA) XP_024302678.1:n.631-4C>A
XM_024446911.1:c.526-4C>A (CRPPA) XP_024302679.1:n.526-4C>A
XR_001744864.1:n.1039-4C>A (CRPPA)
XR_001744866.1:n.1175-4C>A (CRPPA)
XR_001744868.1:n.942-4C>A (CRPPA)
NM_001101426.4:c.934-4C>A (CRPPA) MANE Select NP_001094896.1:n.934-4C>A
NM_001101417.4:c.784-4C>A (CRPPA) NP_001094887.1:n.784-4C>A
NM_001368197.1:c.829-4C>A (CRPPA) NP_001355126.1:n.829-4C>A
NR_160656.1:n.999-4C>A (CRPPA)