Canonical Allele Identifier: CA1202014307

Gene: CRP

Linked Data

• dbSNP Id: rs1660694837
• gnomAD v3: 1-159712466-AAG-A
• gnomAD v4: 1-159712466-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712468_159712469del , CM000663.2:g.159712468_159712469del	GRCh38
NC_000001.10:g.159682258_159682259del , CM000663.1:g.159682258_159682259del	GRCh37
NC_000001.9:g.157948882_157948883del	NCBI36
NG_013007.1:g.7122_7123del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*1057_*1058del MANE Select	ENSP00000255030.5:n.*1057_*1058del
ENST00000368112.5:c.*349_*350del	ENSP00000357093.1:n.*349_*350del
ENST00000437342.1:c.*349_*350del	ENSP00000402788.1:n.*349_*350del
ENST00000473196.1:n.592_593del
NM_000567.2:c.*1057_*1058del	NP_000558.2:n.*1057_*1058del
XM_011509207.1:c.*349_*350del	XP_011507509.1:n.*349_*350del
NM_001329057.1:c.*349_*350del	NP_001315986.1:n.*349_*350del
NM_001329058.1:c.*123_*124del	NP_001315987.1:n.*123_*124del
NM_000567.3:c.*1057_*1058del MANE Select	NP_000558.2:n.*1057_*1058del
NM_001329057.2:c.*349_*350del	NP_001315986.1:n.*349_*350del
NM_001329058.2:c.*123_*124del	NP_001315987.1:n.*123_*124del
NM_001382703.1:c.*1057_*1058del	NP_001369632.1:n.*1057_*1058del