Canonical Allele Identifier: CA526652261

Gene: CRP

Linked Data

• dbSNP Id: rs536128380
• gnomAD v2: 1-159682663-GA-G
• gnomAD v3: 1-159712873-GA-G
• gnomAD v4: 1-159712873-GA-G
• MyVariant Identifiers: chr1:g.159682664del (hg19) ; chr1:g.159712874del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712880del , CM000663.2:g.159712880del	GRCh38
NC_000001.10:g.159682670del , CM000663.1:g.159682670del	GRCh37
NC_000001.9:g.157949294del	NCBI36
NG_013007.1:g.6716del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*651del MANE Select	ENSP00000255030.5:n.*651del
ENST00000368110.1:c.*23-80del	ENSP00000357091.1:n.*23-80del
ENST00000368111.5:c.*23-294del	ENSP00000357092.1:n.*23-294del
ENST00000368112.5:c.*23-80del	ENSP00000357093.1:n.*23-80del
ENST00000437342.1:c.*23-80del	ENSP00000402788.1:n.*23-80del
ENST00000473196.1:n.266-80del
ENST00000489317.1:n.75-80del
NM_000567.2:c.*651del	NP_000558.2:n.*651del
XM_011509207.1:c.*23-80del	XP_011507509.1:n.*23-80del
NM_001329057.1:c.*23-80del	NP_001315986.1:n.*23-80del
NM_001329058.1:c.*23-306del	NP_001315987.1:n.*23-306del
NM_000567.3:c.*651del MANE Select	NP_000558.2:n.*651del
NM_001329057.2:c.*23-80del	NP_001315986.1:n.*23-80del
NM_001329058.2:c.*23-306del	NP_001315987.1:n.*23-306del
NM_001382703.1:c.*651del	NP_001369632.1:n.*651del