Canonical Allele Identifier: CA1202014298
Gene: CRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712460_159712461delinsGC , CM000663.2:g.159712460_159712461delinsGC GRCh38
NC_000001.10:g.159682250_159682251delinsGC , CM000663.1:g.159682250_159682251delinsGC GRCh37
NC_000001.9:g.157948874_157948875delinsGC NCBI36
NG_013007.1:g.7129_7130delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1064_*1065delinsGC MANE Select ENSP00000255030.5:n.*1064_*1065delinsGC
ENST00000368112.5:c.*356_*357delinsGC ENSP00000357093.1:n.*356_*357delinsGC
ENST00000437342.1:c.*356_*357delinsGC ENSP00000402788.1:n.*356_*357delinsGC
ENST00000473196.1:n.599_600delinsGC
NM_000567.2:c.*1064_*1065delinsGC NP_000558.2:n.*1064_*1065delinsGC
XM_011509207.1:c.*356_*357delinsGC XP_011507509.1:n.*356_*357delinsGC
NM_001329057.1:c.*356_*357delinsGC NP_001315986.1:n.*356_*357delinsGC
NM_001329058.1:c.*130_*131delinsGC NP_001315987.1:n.*130_*131delinsGC
NM_000567.3:c.*1064_*1065delinsGC MANE Select NP_000558.2:n.*1064_*1065delinsGC
NM_001329057.2:c.*356_*357delinsGC NP_001315986.1:n.*356_*357delinsGC
NM_001329058.2:c.*130_*131delinsGC NP_001315987.1:n.*130_*131delinsGC
NM_001382703.1:c.*1064_*1065delinsGC NP_001369632.1:n.*1064_*1065delinsGC