Canonical Allele Identifier: CA1690872227
Gene: CRPPA HGNC NCBI

Linked Data

dbSNP Id: rs1166600485
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.16460342G>T , CM000669.2:g.16460342G>T GRCh38
NC_000007.13:g.16499967G>T , CM000669.1:g.16499967G>T GRCh37
NC_000007.12:g.16466492G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000674759.1:c.-47+36038C>A ENSP00000502749.1:n.-47+36038C>A
ENST00000675257.1:c.-47+36038C>A ENSP00000501664.1:n.-47+36038C>A
XM_011515502.1:c.-47+36038C>A XP_011513804.1:n.-47+36038C>A
XM_011515503.1:c.-47+36038C>A XP_011513805.1:n.-47+36038C>A
XM_011515504.1:c.-47+36038C>A XP_011513806.1:n.-47+36038C>A
XM_011515505.1:c.-47+36038C>A XP_011513807.1:n.-47+36038C>A
XM_011515506.1:c.-47+36038C>A XP_011513808.1:n.-47+36038C>A
XM_011515507.1:c.-47+36038C>A XP_011513809.1:n.-47+36038C>A
XR_927059.1:n.143G>T
XM_024446909.1:c.-47+36038C>A XP_024302677.1:n.-47+36038C>A
XM_024446910.1:c.-47+36038C>A XP_024302678.1:n.-47+36038C>A
XM_024446911.1:c.-47+36038C>A XP_024302679.1:n.-47+36038C>A
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