Canonical Allele Identifier: CA4169585

Gene: CRPPA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.16406048A>T , CM000669.2:g.16406048A>T	GRCh38
NC_000007.13:g.16445673A>T , CM000669.1:g.16445673A>T	GRCh37
NC_000007.12:g.16412198A>T	NCBI36
NG_032690.1:g.20275T>A
NG_032690.2:g.20275T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001101426.4:c.534+13T>A MANE Select	NP_001094896.1:n.534+13T>A
ENST00000407010.7:c.534+13T>A MANE Select	ENSP00000385478.2:n.534+13T>A
NM_001101417.3:c.534+13T>A	NP_001094887.1:n.534+13T>A
NM_001101417.4:c.534+13T>A	NP_001094887.1:n.534+13T>A
NM_001101426.3:c.534+13T>A	NP_001094896.1:n.534+13T>A
NM_001368197.1:c.534+13T>A	NP_001355126.1:n.534+13T>A
NR_160656.1:n.750+13T>A
ENST00000399310.3:c.534+13T>A	ENSP00000382249.3:n.534+13T>A
ENST00000407010.6:c.534+13T>A	ENSP00000385478.2:n.534+13T>A
ENST00000674759.1:c.231+13T>A	ENSP00000502749.1:n.231+13T>A
ENST00000675257.1:c.231+13T>A	ENSP00000501664.1:n.231+13T>A
ENST00000676325.1:c.231+13T>A	ENSP00000502074.1:n.231+13T>A
XM_006715770.2:c.285+13T>A	XP_006715833.1:n.285+13T>A
XM_006715770.3:c.285+13T>A	XP_006715833.1:n.285+13T>A
XM_011515497.1:c.534+13T>A	XP_011513799.1:n.534+13T>A
XM_011515498.1:c.534+13T>A	XP_011513800.1:n.534+13T>A
XM_011515499.1:c.534+13T>A	XP_011513801.1:n.534+13T>A
XM_011515499.2:c.534+13T>A	XP_011513801.1:n.534+13T>A
XM_011515500.1:c.534+13T>A	XP_011513802.1:n.534+13T>A
XM_011515500.2:c.534+13T>A	XP_011513802.1:n.534+13T>A
XM_011515501.1:c.534+13T>A	XP_011513803.1:n.534+13T>A
XM_011515501.2:c.534+13T>A	XP_011513803.1:n.534+13T>A
XM_011515502.1:c.231+13T>A	XP_011513804.1:n.231+13T>A
XM_011515503.1:c.231+13T>A	XP_011513805.1:n.231+13T>A
XM_011515504.1:c.231+13T>A	XP_011513806.1:n.231+13T>A
XM_011515505.1:c.231+13T>A	XP_011513807.1:n.231+13T>A
XM_011515506.1:c.231+13T>A	XP_011513808.1:n.231+13T>A
XM_011515507.1:c.231+13T>A	XP_011513809.1:n.231+13T>A
XM_011515508.1:c.231+13T>A	XP_011513810.1:n.231+13T>A
XM_011515508.2:c.231+13T>A	XP_011513810.1:n.231+13T>A
XM_011515509.1:c.231+13T>A	XP_011513811.1:n.231+13T>A
XM_011515509.2:c.231+13T>A	XP_011513811.1:n.231+13T>A
XM_011515510.1:c.534+13T>A	XP_011513812.1:n.534+13T>A
XM_011515511.1:c.534+13T>A	XP_011513813.1:n.534+13T>A
XM_017012575.1:c.534+13T>A	XP_016868064.1:n.534+13T>A
XM_017012576.1:c.534+13T>A	XP_016868065.1:n.534+13T>A
XM_024446909.1:c.231+13T>A	XP_024302677.1:n.231+13T>A
XM_024446910.1:c.231+13T>A	XP_024302678.1:n.231+13T>A
XM_024446911.1:c.231+13T>A	XP_024302679.1:n.231+13T>A
XM_024446912.1:c.285+13T>A	XP_024302680.1:n.285+13T>A
XR_001744864.1:n.685+13T>A
XR_001744865.1:n.693+13T>A
XR_001744866.1:n.713+13T>A
XR_001744867.1:n.717+13T>A
XR_001744868.1:n.693+13T>A