Canonical Allele Identifier: CA1202014759

Gene: CRP

Linked Data

• dbSNP Id: rs1660709633

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712917del , CM000663.2:g.159712917del	GRCh38
NC_000001.10:g.159682707del , CM000663.1:g.159682707del	GRCh37
NC_000001.9:g.157949331del	NCBI36
NG_013007.1:g.6675del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*610del MANE Select	ENSP00000255030.5:n.*610del
ENST00000368110.1:c.*23-121del	ENSP00000357091.1:n.*23-121del
ENST00000368111.5:c.*23-335del	ENSP00000357092.1:n.*23-335del
ENST00000368112.5:c.*23-121del	ENSP00000357093.1:n.*23-121del
ENST00000437342.1:c.*23-121del	ENSP00000402788.1:n.*23-121del
ENST00000473196.1:n.266-121del
ENST00000489317.1:n.75-121del
NM_000567.2:c.*610del	NP_000558.2:n.*610del
XM_011509207.1:c.*23-121del	XP_011507509.1:n.*23-121del
NM_001329057.1:c.*23-121del	NP_001315986.1:n.*23-121del
NM_001329058.1:c.*23-347del	NP_001315987.1:n.*23-347del
NM_000567.3:c.*610del MANE Select	NP_000558.2:n.*610del
NM_001329057.2:c.*23-121del	NP_001315986.1:n.*23-121del
NM_001329058.2:c.*23-347del	NP_001315987.1:n.*23-347del
NM_001382703.1:c.*610del	NP_001369632.1:n.*610del