Canonical Allele Identifier: CA1008297933

Gene: CRP

Linked Data

• dbSNP Id: rs1660694512
• gnomAD v3: 1-159712460-GC-G
• gnomAD v4: 1-159712460-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712461del , CM000663.2:g.159712461del	GRCh38
NC_000001.10:g.159682251del , CM000663.1:g.159682251del	GRCh37
NC_000001.9:g.157948875del	NCBI36
NG_013007.1:g.7129del

Transcript Alleles

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