Canonical Allele Identifier: CA2648593312

Gene: CRP

Linked Data

• gnomAD v4: 1-159713123-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713126del , CM000663.2:g.159713126del	GRCh38
NC_000001.10:g.159682916del , CM000663.1:g.159682916del	GRCh37
NC_000001.9:g.157949540del	NCBI36
NG_013007.1:g.6466del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*401del MANE Select	ENSP00000255030.5:n.*401del
ENST00000368110.1:c.*23-330del	ENSP00000357091.1:n.*23-330del
ENST00000368111.5:c.*22+379del	ENSP00000357092.1:n.*22+379del
ENST00000368112.5:c.*23-330del	ENSP00000357093.1:n.*23-330del
ENST00000437342.1:c.*23-330del	ENSP00000402788.1:n.*23-330del
ENST00000473196.1:n.266-330del
ENST00000489317.1:n.75-330del
NM_000567.2:c.*401del	NP_000558.2:n.*401del
XM_011509207.1:c.*23-330del	XP_011507509.1:n.*23-330del
NM_001329057.1:c.*23-330del	NP_001315986.1:n.*23-330del
NM_001329058.1:c.*22+379del	NP_001315987.1:n.*22+379del
NM_000567.3:c.*401del MANE Select	NP_000558.2:n.*401del
NM_001329057.2:c.*23-330del	NP_001315986.1:n.*23-330del
NM_001329058.2:c.*22+379del	NP_001315987.1:n.*22+379del
NM_001382703.1:c.*401del	NP_001369632.1:n.*401del