Canonical Allele Identifier: CA31390488
Gene: CRP HGNC NCBI

Linked Data

dbSNP Id: rs555825164
gnomAD v2: 1-159683234-GCGGGAGGTACCAGAGACAGAGACGTGGGGCCCATGCGGTGTAAAAAAC-G
gnomAD v3: 1-159713444-GCGGGAGGTACCAGAGACAGAGACGTGGGGCCCATGCGGTGTAAAAAAC-G
gnomAD v4: 1-159713444-GCGGGAGGTACCAGAGACAGAGACGTGGGGCCCATGCGGTGTAAAAAAC-G
MyVariant Identifiers: chr1:g.159683235_159683282del (hg19) chr1:g.159713445_159713492del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159713456_159713503del , CM000663.2:g.159713456_159713503del GRCh38
NC_000001.10:g.159683246_159683293del , CM000663.1:g.159683246_159683293del GRCh37
NC_000001.9:g.157949870_157949917del NCBI36
NG_013007.1:g.6098_6145del

Transcript Alleles

HGVS Amino-acid Change
ENST00000255030.9:c.*33_*80del MANE Select ENSP00000255030.5:n.*33_*80del
ENST00000368110.1:c.*22+11_*22+58del
ENST00000368111.5:c.*22+11_*22+58del
ENST00000368112.5:c.*22+11_*22+58del
ENST00000437342.1:c.*22+11_*22+58del
ENST00000473196.1:n.265+11_265+58del
ENST00000489317.1:n.74+515_74+562del
NM_000567.2:c.*33_*80del NP_000558.2:n.*33_*80del
XM_011509207.1:c.*22+11_*22+58del
NM_001329057.1:c.*22+11_*22+58del
NM_001329058.1:c.*22+11_*22+58del
NM_000567.3:c.*33_*80del MANE Select NP_000558.2:n.*33_*80del
NM_001329057.2:c.*22+11_*22+58del
NM_001329058.2:c.*22+11_*22+58del
NM_001382703.1:c.*33_*80del NP_001369632.1:n.*33_*80del
Search 100 bp 5'
Search 100 bp 3'