Canonical Allele Identifier: CA2648593411

Gene: CRP

Linked Data

• gnomAD v4: 1-159713268-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713269del , CM000663.2:g.159713269del	GRCh38
NC_000001.10:g.159683059del , CM000663.1:g.159683059del	GRCh37
NC_000001.9:g.157949683del	NCBI36
NG_013007.1:g.6321del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*256del MANE Select	ENSP00000255030.5:n.*256del
ENST00000368110.1:c.*22+234del	ENSP00000357091.1:n.*22+234del
ENST00000368111.5:c.*22+234del	ENSP00000357092.1:n.*22+234del
ENST00000368112.5:c.*22+234del	ENSP00000357093.1:n.*22+234del
ENST00000437342.1:c.*22+234del	ENSP00000402788.1:n.*22+234del
ENST00000473196.1:n.265+234del
ENST00000489317.1:n.75-475del
NM_000567.2:c.*256del	NP_000558.2:n.*256del
XM_011509207.1:c.*22+234del	XP_011507509.1:n.*22+234del
NM_001329057.1:c.*22+234del	NP_001315986.1:n.*22+234del
NM_001329058.1:c.*22+234del	NP_001315987.1:n.*22+234del
NM_000567.3:c.*256del MANE Select	NP_000558.2:n.*256del
NM_001329057.2:c.*22+234del	NP_001315986.1:n.*22+234del
NM_001329058.2:c.*22+234del	NP_001315987.1:n.*22+234del
NM_001382703.1:c.*256del	NP_001369632.1:n.*256del