Canonical Allele Identifier: CA1008298160

Gene: CRP

Linked Data

• gnomAD v3: 1-159713073-GTGAATGTGGGCAATGCCCTCCTGCTTTCTGGGGGTCATGGGTGGGGAATTAAATAGAAGATCAGCGCTTCCTTC-G
• gnomAD v4: 1-159713073-GTGAATGTGGGCAATGCCCTCCTGCTTTCTGGGGGTCATGGGTGGGGAATTAAATAGAAGATCAGCGCTTCCTTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713075_159713148del , CM000663.2:g.159713075_159713148del	GRCh38
NC_000001.10:g.159682865_159682938del , CM000663.1:g.159682865_159682938del	GRCh37
NC_000001.9:g.157949489_157949562del	NCBI36
NG_013007.1:g.6443_6516del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*378_*451del MANE Select	ENSP00000255030.5:n.*378_*451del
ENST00000368110.1:c.*23-353_*23-280del	ENSP00000357091.1:n.*23-353_*23-280del
ENST00000368111.5:c.*22+356_*22+429del	ENSP00000357092.1:n.*22+356_*22+429del
ENST00000368112.5:c.*23-353_*23-280del	ENSP00000357093.1:n.*23-353_*23-280del
ENST00000437342.1:c.*23-353_*23-280del	ENSP00000402788.1:n.*23-353_*23-280del
ENST00000473196.1:n.266-353_266-280del
ENST00000489317.1:n.75-353_75-280del
NM_000567.2:c.*378_*451del	NP_000558.2:n.*378_*451del
XM_011509207.1:c.*23-353_*23-280del	XP_011507509.1:n.*23-353_*23-280del
NM_001329057.1:c.*23-353_*23-280del	NP_001315986.1:n.*23-353_*23-280del
NM_001329058.1:c.*22+356_*22+429del	NP_001315987.1:n.*22+356_*22+429del
NM_000567.3:c.*378_*451del MANE Select	NP_000558.2:n.*378_*451del
NM_001329057.2:c.*23-353_*23-280del	NP_001315986.1:n.*23-353_*23-280del
NM_001329058.2:c.*22+356_*22+429del	NP_001315987.1:n.*22+356_*22+429del
NM_001382703.1:c.*378_*451del	NP_001369632.1:n.*378_*451del