Canonical Allele Identifier: CA343453535

Gene: CRP

Linked Data

• gnomAD v4: 1-159713597-A-C
• MyVariant Identifiers: chr1:g.159683387A>C (hg19) ; chr1:g.159713597A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713597A>C , CM000663.2:g.159713597A>C	GRCh38
NC_000001.10:g.159683387A>C , CM000663.1:g.159683387A>C	GRCh37
NC_000001.9:g.157950011A>C	NCBI36
NG_013007.1:g.5993T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.603T>G MANE Select	ENSP00000255030.5:p.Asn201Lys
ENST00000368110.1:c.237T>G	ENSP00000357091.1:p.Asn79Lys
ENST00000368111.5:c.237T>G	ENSP00000357092.1:p.Asn79Lys
ENST00000368112.5:c.204T>G	ENSP00000357093.1:p.Asn68Lys
ENST00000437342.1:c.69T>G	ENSP00000402788.1:p.Asn23Lys
ENST00000473196.1:n.171T>G
ENST00000489317.1:n.74+410T>G
NM_000567.2:c.603T>G	NP_000558.2:p.Asn201Lys
XM_011509207.1:c.603T>G	XP_011507509.1:p.Asn201Lys
NM_001329057.1:c.603T>G	NP_001315986.1:p.Asn201Lys
NM_001329058.1:c.204T>G	NP_001315987.1:p.Asn68Lys
NM_000567.3:c.603T>G MANE Select	NP_000558.2:p.Asn201Lys
NM_001329057.2:c.603T>G	NP_001315986.1:p.Asn201Lys
NM_001329058.2:c.204T>G	NP_001315987.1:p.Asn68Lys
NM_001382703.1:c.237T>G	NP_001369632.1:p.Asn79Lys