Canonical Allele Identifier: CA1690872299

Gene: CRPPA

Linked Data

• dbSNP Id: rs1490129108

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.16460428G>A , CM000669.2:g.16460428G>A	GRCh38
NC_000007.13:g.16500053G>A , CM000669.1:g.16500053G>A	GRCh37
NC_000007.12:g.16466578G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000674759.1:c.-47+35952C>T	ENSP00000502749.1:n.-47+35952C>T
ENST00000675257.1:c.-47+35952C>T	ENSP00000501664.1:n.-47+35952C>T
XM_011515502.1:c.-47+35952C>T	XP_011513804.1:n.-47+35952C>T
XM_011515503.1:c.-47+35952C>T	XP_011513805.1:n.-47+35952C>T
XM_011515504.1:c.-47+35952C>T	XP_011513806.1:n.-47+35952C>T
XM_011515505.1:c.-47+35952C>T	XP_011513807.1:n.-47+35952C>T
XM_011515506.1:c.-47+35952C>T	XP_011513808.1:n.-47+35952C>T
XM_011515507.1:c.-47+35952C>T	XP_011513809.1:n.-47+35952C>T
XR_927059.1:n.229G>A
XM_024446909.1:c.-47+35952C>T	XP_024302677.1:n.-47+35952C>T
XM_024446910.1:c.-47+35952C>T	XP_024302678.1:n.-47+35952C>T
XM_024446911.1:c.-47+35952C>T	XP_024302679.1:n.-47+35952C>T