Canonical Allele Identifier: CA1008298985

Gene: CRP

Linked Data

• dbSNP Id: rs1660779327
• gnomAD v3: 1-159714486-G-T
• gnomAD v4: 1-159714486-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159714486G>T , CM000663.2:g.159714486G>T	GRCh38
NC_000001.10:g.159684276G>T , CM000663.1:g.159684276G>T	GRCh37
NC_000001.9:g.157950900G>T	NCBI36
NG_013007.1:g.5104C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.-1C>A MANE Select	ENSP00000255030.5:n.-1C>A
ENST00000368110.1:c.-1C>A	ENSP00000357091.1:n.-1C>A
ENST00000368111.5:c.-1C>A	ENSP00000357092.1:n.-1C>A
ENST00000368112.5:c.-1C>A	ENSP00000357093.1:n.-1C>A
ENST00000437342.1:c.-308+13C>A	ENSP00000402788.1:n.-308+13C>A
NM_000567.2:c.-1C>A	NP_000558.2:n.-1C>A
XM_011509207.1:c.-1C>A	XP_011507509.1:n.-1C>A
NM_001329057.1:c.-1C>A	NP_001315986.1:n.-1C>A
NM_001329058.1:c.-1C>A	NP_001315987.1:n.-1C>A
NM_000567.3:c.-1C>A MANE Select	NP_000558.2:n.-1C>A
NM_001329057.2:c.-1C>A	NP_001315986.1:n.-1C>A
NM_001329058.2:c.-1C>A	NP_001315987.1:n.-1C>A
NM_001382703.1:c.-1C>A	NP_001369632.1:n.-1C>A