Canonical Allele Identifier: CA343454345

Gene: CRP

Linked Data

• MyVariant Identifiers: chr1:g.159683659G>T (hg19) ; chr1:g.159713869G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713869G>T , CM000663.2:g.159713869G>T	GRCh38
NC_000001.10:g.159683659G>T , CM000663.1:g.159683659G>T	GRCh37
NC_000001.9:g.157950283G>T	NCBI36
NG_013007.1:g.5721C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.331C>A MANE Select	ENSP00000255030.5:p.Pro111Thr
ENST00000368110.1:c.193+138C>A	ENSP00000357091.1:n.193+138C>A
ENST00000368111.5:c.193+138C>A	ENSP00000357092.1:n.193+138C>A
ENST00000368112.5:c.197+134C>A	ENSP00000357093.1:n.197+134C>A
ENST00000437342.1:c.-204C>A	ENSP00000402788.1:n.-204C>A
ENST00000489317.1:n.74+138C>A
NM_000567.2:c.331C>A	NP_000558.2:p.Pro111Thr
XM_011509207.1:c.331C>A	XP_011507509.1:p.Pro111Thr
NM_001329057.1:c.331C>A	NP_001315986.1:p.Pro111Thr
NM_001329058.1:c.197+134C>A	NP_001315987.1:n.197+134C>A
NM_000567.3:c.331C>A MANE Select	NP_000558.2:p.Pro111Thr
NM_001329057.2:c.331C>A	NP_001315986.1:p.Pro111Thr
NM_001329058.2:c.197+134C>A	NP_001315987.1:n.197+134C>A
NM_001382703.1:c.193+138C>A	NP_001369632.1:n.193+138C>A