Canonical Allele Identifier: CA2648592893
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712443_159712444del , CM000663.2:g.159712443_159712444del GRCh38
NC_000001.10:g.159682233_159682234del , CM000663.1:g.159682233_159682234del GRCh37
NC_000001.9:g.157948857_157948858del NCBI36
NG_013007.1:g.7148_7149del

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1083_*1084del MANE Select ENSP00000255030.5:n.*1083_*1084del
ENST00000368112.5:c.*375_*376del ENSP00000357093.1:n.*375_*376del
ENST00000437342.1:c.*375_*376del ENSP00000402788.1:n.*375_*376del
ENST00000473196.1:n.618_619del
NM_000567.2:c.*1083_*1084del NP_000558.2:n.*1083_*1084del
XM_011509207.1:c.*375_*376del XP_011507509.1:n.*375_*376del
NM_001329057.1:c.*375_*376del NP_001315986.1:n.*375_*376del
NM_001329058.1:c.*149_*150del NP_001315987.1:n.*149_*150del
NM_000567.3:c.*1083_*1084del MANE Select NP_000558.2:n.*1083_*1084del
NM_001329057.2:c.*375_*376del NP_001315986.1:n.*375_*376del
NM_001329058.2:c.*149_*150del NP_001315987.1:n.*149_*150del
NM_001382703.1:c.*1083_*1084del NP_001369632.1:n.*1083_*1084del