Canonical Allele Identifier: CA10628802

Gene: CRPPA

Linked Data

• ClinVar Variation Id: 359587
• ClinVar RCV Id: RCV000387775 ; RCV002229906
• dbSNP Id: rs376232862
• gnomAD v4: 7-16376080-C-T
• MyVariant Identifiers: chr7:g.16415705C>T (hg19) ; chr7:g.16376080C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.16376080C>T , CM000669.2:g.16376080C>T	GRCh38
NC_000007.13:g.16415705C>T , CM000669.1:g.16415705C>T	GRCh37
NC_000007.12:g.16382230C>T	NCBI36
NG_032690.1:g.50243G>A
NG_032690.2:g.50243G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407010.7:c.684+12G>A MANE Select	ENSP00000385478.2:n.684+12G>A
ENST00000674759.1:c.381+12G>A	ENSP00000502749.1:n.381+12G>A
ENST00000675257.1:c.381+12G>A	ENSP00000501664.1:n.381+12G>A
ENST00000676325.1:c.381+12G>A	ENSP00000502074.1:n.381+12G>A
ENST00000399310.3:c.534+29981G>A	ENSP00000382249.3:n.534+29981G>A
ENST00000407010.6:c.684+12G>A	ENSP00000385478.2:n.684+12G>A
NM_001101417.3:c.534+29981G>A	NP_001094887.1:n.534+29981G>A
NM_001101426.3:c.684+12G>A	NP_001094896.1:n.684+12G>A
XM_006715770.2:c.435+12G>A	XP_006715833.1:n.435+12G>A
XM_011515497.1:c.684+12G>A	XP_011513799.1:n.684+12G>A
XM_011515498.1:c.684+12G>A	XP_011513800.1:n.684+12G>A
XM_011515499.1:c.684+12G>A	XP_011513801.1:n.684+12G>A
XM_011515500.1:c.684+12G>A	XP_011513802.1:n.684+12G>A
XM_011515501.1:c.684+12G>A	XP_011513803.1:n.684+12G>A
XM_011515502.1:c.381+12G>A	XP_011513804.1:n.381+12G>A
XM_011515503.1:c.381+12G>A	XP_011513805.1:n.381+12G>A
XM_011515504.1:c.381+12G>A	XP_011513806.1:n.381+12G>A
XM_011515505.1:c.381+12G>A	XP_011513807.1:n.381+12G>A
XM_011515506.1:c.381+12G>A	XP_011513808.1:n.381+12G>A
XM_011515507.1:c.381+12G>A	XP_011513809.1:n.381+12G>A
XM_011515508.1:c.381+12G>A	XP_011513810.1:n.381+12G>A
XM_011515509.1:c.381+12G>A	XP_011513811.1:n.381+12G>A
XM_011515510.1:c.684+12G>A	XP_011513812.1:n.684+12G>A
XM_011515511.1:c.684+12G>A	XP_011513813.1:n.684+12G>A
XM_006715770.3:c.435+12G>A	XP_006715833.1:n.435+12G>A
XM_011515499.2:c.684+12G>A	XP_011513801.1:n.684+12G>A
XM_011515500.2:c.684+12G>A	XP_011513802.1:n.684+12G>A
XM_011515501.2:c.684+12G>A	XP_011513803.1:n.684+12G>A
XM_011515508.2:c.381+12G>A	XP_011513810.1:n.381+12G>A
XM_011515509.2:c.381+12G>A	XP_011513811.1:n.381+12G>A
XM_017012575.1:c.684+12G>A	XP_016868064.1:n.684+12G>A
XM_017012576.1:c.684+12G>A	XP_016868065.1:n.684+12G>A
XM_017012577.1:c.48+12G>A	XP_016868066.1:n.48+12G>A
XM_024446909.1:c.381+12G>A	XP_024302677.1:n.381+12G>A
XM_024446910.1:c.381+12G>A	XP_024302678.1:n.381+12G>A
XM_024446911.1:c.381+12G>A	XP_024302679.1:n.381+12G>A
XM_024446912.1:c.435+12G>A	XP_024302680.1:n.435+12G>A
XR_001744864.1:n.835+12G>A
XR_001744865.1:n.843+12G>A
XR_001744866.1:n.863+12G>A
XR_001744867.1:n.867+12G>A
XR_001744868.1:n.843+12G>A
NM_001101426.4:c.684+12G>A MANE Select	NP_001094896.1:n.684+12G>A
NM_001101417.4:c.534+29981G>A	NP_001094887.1:n.534+29981G>A
NM_001368197.1:c.684+12G>A	NP_001355126.1:n.684+12G>A
NR_160656.1:n.900+12G>A