Canonical Allele Identifier: CA2648593135

Gene: CRP

Linked Data

• gnomAD v4: 1-159712896-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712900del , CM000663.2:g.159712900del	GRCh38
NC_000001.10:g.159682690del , CM000663.1:g.159682690del	GRCh37
NC_000001.9:g.157949314del	NCBI36
NG_013007.1:g.6693del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*628del MANE Select	ENSP00000255030.5:n.*628del
ENST00000368110.1:c.*23-103del	ENSP00000357091.1:n.*23-103del
ENST00000368111.5:c.*23-317del	ENSP00000357092.1:n.*23-317del
ENST00000368112.5:c.*23-103del	ENSP00000357093.1:n.*23-103del
ENST00000437342.1:c.*23-103del	ENSP00000402788.1:n.*23-103del
ENST00000473196.1:n.266-103del
ENST00000489317.1:n.75-103del
NM_000567.2:c.*628del	NP_000558.2:n.*628del
XM_011509207.1:c.*23-103del	XP_011507509.1:n.*23-103del
NM_001329057.1:c.*23-103del	NP_001315986.1:n.*23-103del
NM_001329058.1:c.*23-329del	NP_001315987.1:n.*23-329del
NM_000567.3:c.*628del MANE Select	NP_000558.2:n.*628del
NM_001329057.2:c.*23-103del	NP_001315986.1:n.*23-103del
NM_001329058.2:c.*23-329del	NP_001315987.1:n.*23-329del
NM_001382703.1:c.*628del	NP_001369632.1:n.*628del