Canonical Allele Identifier: CA890067379

Gene: CRP

Linked Data

• dbSNP Id: rs1444101754
• gnomAD v3: 1-159713217-T-A
• gnomAD v4: 1-159713217-T-A
• MyVariant Identifiers: chr1:g.159683007T>A (hg19) ; chr1:g.159713217T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713217T>A , CM000663.2:g.159713217T>A	GRCh38
NC_000001.10:g.159683007T>A , CM000663.1:g.159683007T>A	GRCh37
NC_000001.9:g.157949631T>A	NCBI36
NG_013007.1:g.6373A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*308A>T MANE Select	ENSP00000255030.5:n.*308A>T
ENST00000368110.1:c.*22+286A>T	ENSP00000357091.1:n.*22+286A>T
ENST00000368111.5:c.*22+286A>T	ENSP00000357092.1:n.*22+286A>T
ENST00000368112.5:c.*22+286A>T	ENSP00000357093.1:n.*22+286A>T
ENST00000437342.1:c.*22+286A>T	ENSP00000402788.1:n.*22+286A>T
ENST00000473196.1:n.265+286A>T
ENST00000489317.1:n.75-423A>T
NM_000567.2:c.*308A>T	NP_000558.2:n.*308A>T
XM_011509207.1:c.*22+286A>T	XP_011507509.1:n.*22+286A>T
NM_001329057.1:c.*22+286A>T	NP_001315986.1:n.*22+286A>T
NM_001329058.1:c.*22+286A>T	NP_001315987.1:n.*22+286A>T
NM_000567.3:c.*308A>T MANE Select	NP_000558.2:n.*308A>T
NM_001329057.2:c.*22+286A>T	NP_001315986.1:n.*22+286A>T
NM_001329058.2:c.*22+286A>T	NP_001315987.1:n.*22+286A>T
NM_001382703.1:c.*308A>T	NP_001369632.1:n.*308A>T