Canonical Allele Identifier: CA2648592730
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712344_159712345insCGAT , CM000663.2:g.159712344_159712345insCGAT GRCh38
NC_000001.10:g.159682134_159682135insCGAT , CM000663.1:g.159682134_159682135insCGAT GRCh37
NC_000001.9:g.157948758_157948759insCGAT NCBI36
NG_013007.1:g.7246_7247insTCGA

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1181_*1182insTCGA MANE Select ENSP00000255030.5:n.*1181_*1182insTCGA
ENST00000437342.1:c.*473_*474insTCGA ENSP00000402788.1:n.*473_*474insTCGA
ENST00000473196.1:n.716_717insTCGA
NM_000567.2:c.*1181_*1182insTCGA NP_000558.2:n.*1181_*1182insTCGA
XM_011509207.1:c.*473_*474insTCGA XP_011507509.1:n.*473_*474insTCGA
NM_001329057.1:c.*473_*474insTCGA NP_001315986.1:n.*473_*474insTCGA
NM_001329058.1:c.*247_*248insTCGA NP_001315987.1:n.*247_*248insTCGA
NM_000567.3:c.*1181_*1182insTCGA MANE Select NP_000558.2:n.*1181_*1182insTCGA
NM_001329057.2:c.*473_*474insTCGA NP_001315986.1:n.*473_*474insTCGA
NM_001329058.2:c.*247_*248insTCGA NP_001315987.1:n.*247_*248insTCGA
NM_001382703.1:c.*1181_*1182insTCGA NP_001369632.1:n.*1181_*1182insTCGA