Canonical Allele Identifier: CA343453993
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159713725A>G , CM000663.2:g.159713725A>G GRCh38
NC_000001.10:g.159683515A>G , CM000663.1:g.159683515A>G GRCh37
NC_000001.9:g.157950139A>G NCBI36
NG_013007.1:g.5865T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000255030.9:c.475T>C MANE Select ENSP00000255030.5:p.Ser159Pro
ENST00000368110.1:c.194-85T>C ENSP00000357091.1:n.194-85T>C
ENST00000368111.5:c.194-85T>C ENSP00000357092.1:n.194-85T>C
ENST00000368112.5:c.198-122T>C ENSP00000357093.1:n.198-122T>C
ENST00000437342.1:c.-60T>C ENSP00000402788.1:n.-60T>C
ENST00000473196.1:n.43T>C
ENST00000489317.1:n.74+282T>C
NM_000567.2:c.475T>C NP_000558.2:p.Ser159Pro
XM_011509207.1:c.475T>C XP_011507509.1:p.Ser159Pro
NM_001329057.1:c.475T>C NP_001315986.1:p.Ser159Pro
NM_001329058.1:c.198-122T>C NP_001315987.1:n.198-122T>C
NM_000567.3:c.475T>C MANE Select NP_000558.2:p.Ser159Pro
NM_001329057.2:c.475T>C NP_001315986.1:p.Ser159Pro
NM_001329058.2:c.198-122T>C NP_001315987.1:n.198-122T>C
NM_001382703.1:c.194-85T>C NP_001369632.1:n.194-85T>C