Canonical Allele Identifier: CA2648593475
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159713301_159713302insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGCA , CM000663.2:g.159713301_159713302insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGCA GRCh38
NC_000001.10:g.159683091_159683092insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGCA , CM000663.1:g.159683091_159683092insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGCA GRCh37
NC_000001.9:g.157949715_157949716insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGCA NCBI36
NG_013007.1:g.6288_6289insTGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*223_*224insTGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC MANE Select ENSP00000255030.5:n.*223_*224insTGCCCCCCC...
ENST00000368110.1:c.*22+201_*22+202insTGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC ENSP00000357091.1:n.*22+201_*22+202insTGC...
ENST00000368111.5:c.*22+201_*22+202insTGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC ENSP00000357092.1:n.*22+201_*22+202insTGC...
ENST00000368112.5:c.*22+201_*22+202insTGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC ENSP00000357093.1:n.*22+201_*22+202insTGC...
ENST00000437342.1:c.*22+201_*22+202insTGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC ENSP00000402788.1:n.*22+201_*22+202insTGC...
ENST00000473196.1:n.265+201_265+202insTGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
ENST00000489317.1:n.75-508_75-507insTGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
NM_000567.2:c.*223_*224insTGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC NP_000558.2:n.*223_*224insTGCCCCCCCCCCCCC...
XM_011509207.1:c.*22+201_*22+202insTGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC XP_011507509.1:n.*22+201_*22+202insTGCCCC...
NM_001329057.1:c.*22+201_*22+202insTGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC NP_001315986.1:n.*22+201_*22+202insTGCCCC...
NM_001329058.1:c.*22+201_*22+202insTGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC NP_001315987.1:n.*22+201_*22+202insTGCCCC...
NM_000567.3:c.*223_*224insTGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC MANE Select NP_000558.2:n.*223_*224insTGCCCCCCCCCCCCC...
NM_001329057.2:c.*22+201_*22+202insTGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC NP_001315986.1:n.*22+201_*22+202insTGCCCC...
NM_001329058.2:c.*22+201_*22+202insTGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC NP_001315987.1:n.*22+201_*22+202insTGCCCC...
NM_001382703.1:c.*223_*224insTGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC NP_001369632.1:n.*223_*224insTGCCCCCCCCCC...