Canonical Allele Identifier: CA2566014666
Gene: CRPPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.16460738_16460739del , CM000669.2:g.16460738_16460739del GRCh38
NC_000007.13:g.16500363_16500364del , CM000669.1:g.16500363_16500364del GRCh37
NC_000007.12:g.16466888_16466889del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000674759.1:c.-47+35642_-47+35643del ENSP00000502749.1:n.-47+35642_-47+35643del
ENST00000675257.1:c.-47+35642_-47+35643del ENSP00000501664.1:n.-47+35642_-47+35643del
XM_011515502.1:c.-47+35642_-47+35643del XP_011513804.1:n.-47+35642_-47+35643del
XM_011515503.1:c.-47+35642_-47+35643del XP_011513805.1:n.-47+35642_-47+35643del
XM_011515504.1:c.-47+35642_-47+35643del XP_011513806.1:n.-47+35642_-47+35643del
XM_011515505.1:c.-47+35642_-47+35643del XP_011513807.1:n.-47+35642_-47+35643del
XM_011515506.1:c.-47+35642_-47+35643del XP_011513808.1:n.-47+35642_-47+35643del
XM_011515507.1:c.-47+35642_-47+35643del XP_011513809.1:n.-47+35642_-47+35643del
XR_927059.1:n.539_540del
XM_024446909.1:c.-47+35642_-47+35643del XP_024302677.1:n.-47+35642_-47+35643del
XM_024446910.1:c.-47+35642_-47+35643del XP_024302678.1:n.-47+35642_-47+35643del
XM_024446911.1:c.-47+35642_-47+35643del XP_024302679.1:n.-47+35642_-47+35643del