Canonical Allele Identifier: CA1690873635

Gene: CRPPA

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.16421142_16421143dup , CM000669.2:g.16421142_16421143dup	GRCh38
NC_000007.13:g.16460767_16460768dup , CM000669.1:g.16460767_16460768dup	GRCh37
NC_000007.12:g.16427292_16427293dup	NCBI36
NG_032690.1:g.5183_5184dup
NG_032690.2:g.5183_5184dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407010.7:c.183_184dup MANE Select	ENSP00000385478.2:p.Val62GlyfsTer30
ENST00000674759.1:c.-46-14803_-46-14802dup	ENSP00000502749.1:n.-46-14803_-46-14802dup
ENST00000675257.1:c.-46-14803_-46-14802dup	ENSP00000501664.1:n.-46-14803_-46-14802dup
ENST00000399310.3:c.183_184dup	ENSP00000382249.3:p.Val62GlyfsTer30
ENST00000407010.6:c.183_184dup	ENSP00000385478.2:p.Val62GlyfsTer30
NM_001101417.3:c.183_184dup	NP_001094887.1:p.Val62GlyfsTer30
NM_001101426.3:c.183_184dup	NP_001094896.1:p.Val62GlyfsTer30
XM_011515497.1:c.183_184dup	XP_011513799.1:p.Val62GlyfsTer30
XM_011515498.1:c.183_184dup	XP_011513800.1:p.Val62GlyfsTer30
XM_011515499.1:c.183_184dup	XP_011513801.1:p.Val62GlyfsTer30
XM_011515500.1:c.183_184dup	XP_011513802.1:p.Val62GlyfsTer30
XM_011515501.1:c.183_184dup	XP_011513803.1:p.Val62GlyfsTer30
XM_011515502.1:c.-46-14803_-46-14802dup	XP_011513804.1:n.-46-14803_-46-14802dup
XM_011515503.1:c.-46-14803_-46-14802dup	XP_011513805.1:n.-46-14803_-46-14802dup
XM_011515504.1:c.-46-14803_-46-14802dup	XP_011513806.1:n.-46-14803_-46-14802dup
XM_011515505.1:c.-46-14803_-46-14802dup	XP_011513807.1:n.-46-14803_-46-14802dup
XM_011515506.1:c.-46-14803_-46-14802dup	XP_011513808.1:n.-46-14803_-46-14802dup
XM_011515507.1:c.-46-14803_-46-14802dup	XP_011513809.1:n.-46-14803_-46-14802dup
XM_011515508.1:c.-47+664_-47+665dup	XP_011513810.1:n.-47+664_-47+665dup
XM_011515510.1:c.183_184dup	XP_011513812.1:p.Val62GlyfsTer30
XM_011515511.1:c.183_184dup	XP_011513813.1:p.Val62GlyfsTer30
XM_011515499.2:c.183_184dup	XP_011513801.1:p.Val62GlyfsTer30
XM_011515500.2:c.183_184dup	XP_011513802.1:p.Val62GlyfsTer30
XM_011515501.2:c.183_184dup	XP_011513803.1:p.Val62GlyfsTer30
XM_011515508.2:c.-47+664_-47+665dup	XP_011513810.1:n.-47+664_-47+665dup
XM_017012575.1:c.183_184dup	XP_016868064.1:p.Val62GlyfsTer30
XM_017012576.1:c.183_184dup	XP_016868065.1:p.Val62GlyfsTer30
XM_024446909.1:c.-46-14803_-46-14802dup	XP_024302677.1:n.-46-14803_-46-14802dup
XM_024446910.1:c.-46-14803_-46-14802dup	XP_024302678.1:n.-46-14803_-46-14802dup
XM_024446911.1:c.-46-14803_-46-14802dup	XP_024302679.1:n.-46-14803_-46-14802dup
XR_001744864.1:n.334_335dup
XR_001744865.1:n.342_343dup
XR_001744866.1:n.362_363dup
XR_001744867.1:n.366_367dup
XR_001744868.1:n.342_343dup
NM_001101426.4:c.183_184dup MANE Select	NP_001094896.1:p.Val62GlyfsTer30
NM_001101417.4:c.183_184dup	NP_001094887.1:p.Val62GlyfsTer30
NM_001368197.1:c.183_184dup	NP_001355126.1:p.Val62GlyfsTer30
NR_160656.1:n.399_400dup