Canonical Allele Identifier: CA2713878938
Gene: CRPPA HGNC NCBI

Linked Data

dbSNP Id: rs1781194812

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.16460356C>G , CM000669.2:g.16460356C>G GRCh38
NC_000007.13:g.16499981C>G , CM000669.1:g.16499981C>G GRCh37
NC_000007.12:g.16466506C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000674759.1:c.-47+36024G>C ENSP00000502749.1:n.-47+36024G>C
ENST00000675257.1:c.-47+36024G>C ENSP00000501664.1:n.-47+36024G>C
XM_011515502.1:c.-47+36024G>C XP_011513804.1:n.-47+36024G>C
XM_011515503.1:c.-47+36024G>C XP_011513805.1:n.-47+36024G>C
XM_011515504.1:c.-47+36024G>C XP_011513806.1:n.-47+36024G>C
XM_011515505.1:c.-47+36024G>C XP_011513807.1:n.-47+36024G>C
XM_011515506.1:c.-47+36024G>C XP_011513808.1:n.-47+36024G>C
XM_011515507.1:c.-47+36024G>C XP_011513809.1:n.-47+36024G>C
XR_927059.1:n.157C>G
XM_024446909.1:c.-47+36024G>C XP_024302677.1:n.-47+36024G>C
XM_024446910.1:c.-47+36024G>C XP_024302678.1:n.-47+36024G>C
XM_024446911.1:c.-47+36024G>C XP_024302679.1:n.-47+36024G>C