Canonical Allele Identifier: CA1202015033

Gene: CRP

Linked Data

• dbSNP Id: rs1345218671
• gnomAD v4: 1-159713221-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713221G>A , CM000663.2:g.159713221G>A	GRCh38
NC_000001.10:g.159683011G>A , CM000663.1:g.159683011G>A	GRCh37
NC_000001.9:g.157949635G>A	NCBI36
NG_013007.1:g.6369C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*304C>T MANE Select	ENSP00000255030.5:n.*304C>T
ENST00000368110.1:c.*22+282C>T	ENSP00000357091.1:n.*22+282C>T
ENST00000368111.5:c.*22+282C>T	ENSP00000357092.1:n.*22+282C>T
ENST00000368112.5:c.*22+282C>T	ENSP00000357093.1:n.*22+282C>T
ENST00000437342.1:c.*22+282C>T	ENSP00000402788.1:n.*22+282C>T
ENST00000473196.1:n.265+282C>T
ENST00000489317.1:n.75-427C>T
NM_000567.2:c.*304C>T	NP_000558.2:n.*304C>T
XM_011509207.1:c.*22+282C>T	XP_011507509.1:n.*22+282C>T
NM_001329057.1:c.*22+282C>T	NP_001315986.1:n.*22+282C>T
NM_001329058.1:c.*22+282C>T	NP_001315987.1:n.*22+282C>T
NM_000567.3:c.*304C>T MANE Select	NP_000558.2:n.*304C>T
NM_001329057.2:c.*22+282C>T	NP_001315986.1:n.*22+282C>T
NM_001329058.2:c.*22+282C>T	NP_001315987.1:n.*22+282C>T
NM_001382703.1:c.*304C>T	NP_001369632.1:n.*304C>T