Canonical Allele Identifier: CA367000686

Gene: CRPPA CRPPA-AS1

Linked Data

• ClinVar Variation Id: 450705
• ClinVar RCV Id: RCV000520716
• dbSNP Id: rs1554300301
• MyVariant Identifiers: chr7:g.16298544C>A (hg19) ; chr7:g.16258919C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.16258919C>A , CM000669.2:g.16258919C>A	GRCh38
NC_000007.13:g.16298544C>A , CM000669.1:g.16298544C>A	GRCh37
NC_000007.12:g.16265069C>A	NCBI36
NG_032690.1:g.167404G>T
NG_032690.2:g.167404G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407010.7:c.1026+1G>T (CRPPA) MANE Select	ENSP00000385478.2:n.1026+1G>T
ENST00000674759.1:c.723+1G>T (CRPPA)	ENSP00000502749.1:n.723+1G>T
ENST00000675257.1:c.618+1G>T (CRPPA)	ENSP00000501664.1:n.618+1G>T
ENST00000676325.1:c.723+1G>T (CRPPA)	ENSP00000502074.1:n.723+1G>T
ENST00000399310.3:c.876+1G>T (CRPPA)	ENSP00000382249.3:n.876+1G>T
ENST00000407010.6:c.1026+1G>T (CRPPA)	ENSP00000385478.2:n.1026+1G>T
NM_001101417.3:c.876+1G>T (CRPPA)	NP_001094887.1:n.876+1G>T
NM_001101426.3:c.1026+1G>T (CRPPA)	NP_001094896.1:n.1026+1G>T
NR_038946.1:n.224-2980C>A (CRPPA-AS1)
NR_038947.1:n.241-7308C>A (CRPPA-AS1)
XM_006715770.2:c.777+1G>T (CRPPA)	XP_006715833.1:n.777+1G>T
XM_011515497.1:c.1026+1G>T (CRPPA)	XP_011513799.1:n.1026+1G>T
XM_011515498.1:c.1026+1G>T (CRPPA)	XP_011513800.1:n.1026+1G>T
XM_011515499.1:c.1026+1G>T (CRPPA)	XP_011513801.1:n.1026+1G>T
XM_011515500.1:c.921+1G>T (CRPPA)	XP_011513802.1:n.921+1G>T
XM_011515502.1:c.723+1G>T (CRPPA)	XP_011513804.1:n.723+1G>T
XM_011515503.1:c.723+1G>T (CRPPA)	XP_011513805.1:n.723+1G>T
XM_011515504.1:c.723+1G>T (CRPPA)	XP_011513806.1:n.723+1G>T
XM_011515505.1:c.723+1G>T (CRPPA)	XP_011513807.1:n.723+1G>T
XM_011515506.1:c.723+1G>T (CRPPA)	XP_011513808.1:n.723+1G>T
XM_011515507.1:c.723+1G>T (CRPPA)	XP_011513809.1:n.723+1G>T
XM_011515508.1:c.723+1G>T (CRPPA)	XP_011513810.1:n.723+1G>T
XM_011515509.1:c.723+1G>T (CRPPA)	XP_011513811.1:n.723+1G>T
XM_006715770.3:c.777+1G>T (CRPPA)	XP_006715833.1:n.777+1G>T
XM_011515499.2:c.1026+1G>T (CRPPA)	XP_011513801.1:n.1026+1G>T
XM_011515500.2:c.921+1G>T (CRPPA)	XP_011513802.1:n.921+1G>T
XM_011515508.2:c.723+1G>T (CRPPA)	XP_011513810.1:n.723+1G>T
XM_011515509.2:c.723+1G>T (CRPPA)	XP_011513811.1:n.723+1G>T
XM_017012575.1:c.1026+1G>T (CRPPA)	XP_016868064.1:n.1026+1G>T
XM_017012577.1:c.390+1G>T (CRPPA)	XP_016868066.1:n.390+1G>T
XM_017012578.1:c.390+1G>T (CRPPA)	XP_016868067.1:n.390+1G>T
XM_024446909.1:c.723+1G>T (CRPPA)	XP_024302677.1:n.723+1G>T
XM_024446910.1:c.723+1G>T (CRPPA)	XP_024302678.1:n.723+1G>T
XM_024446911.1:c.618+1G>T (CRPPA)	XP_024302679.1:n.618+1G>T
XR_001744866.1:n.1267+1G>T (CRPPA)
XR_001744868.1:n.1034+1G>T (CRPPA)
NM_001101426.4:c.1026+1G>T (CRPPA) MANE Select	NP_001094896.1:n.1026+1G>T
NM_001101417.4:c.876+1G>T (CRPPA)	NP_001094887.1:n.876+1G>T
NM_001368197.1:c.921+1G>T (CRPPA)	NP_001355126.1:n.921+1G>T
NR_160656.1:n.1091+1G>T (CRPPA)