Canonical Allele Identifier: CA343454089
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159713751C>A , CM000663.2:g.159713751C>A GRCh38
NC_000001.10:g.159683541C>A , CM000663.1:g.159683541C>A GRCh37
NC_000001.9:g.157950165C>A NCBI36
NG_013007.1:g.5839G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000255030.9:c.449G>T MANE Select ENSP00000255030.5:p.Ser150Ile
ENST00000368110.1:c.194-111G>T ENSP00000357091.1:n.194-111G>T
ENST00000368111.5:c.194-111G>T ENSP00000357092.1:n.194-111G>T
ENST00000368112.5:c.198-148G>T ENSP00000357093.1:n.198-148G>T
ENST00000437342.1:c.-86G>T ENSP00000402788.1:n.-86G>T
ENST00000473196.1:n.17G>T
ENST00000489317.1:n.74+256G>T
NM_000567.2:c.449G>T NP_000558.2:p.Ser150Ile
XM_011509207.1:c.449G>T XP_011507509.1:p.Ser150Ile
NM_001329057.1:c.449G>T NP_001315986.1:p.Ser150Ile
NM_001329058.1:c.198-148G>T NP_001315987.1:n.198-148G>T
NM_000567.3:c.449G>T MANE Select NP_000558.2:p.Ser150Ile
NM_001329057.2:c.449G>T NP_001315986.1:p.Ser150Ile
NM_001329058.2:c.198-148G>T NP_001315987.1:n.198-148G>T
NM_001382703.1:c.194-111G>T NP_001369632.1:n.194-111G>T