Canonical Allele Identifier: CA2648593479

Gene: CRP

Linked Data

• gnomAD v4: 1-159713304-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713304T>A , CM000663.2:g.159713304T>A	GRCh38
NC_000001.10:g.159683094T>A , CM000663.1:g.159683094T>A	GRCh37
NC_000001.9:g.157949718T>A	NCBI36
NG_013007.1:g.6286A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*221A>T MANE Select	ENSP00000255030.5:n.*221A>T
ENST00000368110.1:c.*22+199A>T	ENSP00000357091.1:n.*22+199A>T
ENST00000368111.5:c.*22+199A>T	ENSP00000357092.1:n.*22+199A>T
ENST00000368112.5:c.*22+199A>T	ENSP00000357093.1:n.*22+199A>T
ENST00000437342.1:c.*22+199A>T	ENSP00000402788.1:n.*22+199A>T
ENST00000473196.1:n.265+199A>T
ENST00000489317.1:n.75-510A>T
NM_000567.2:c.*221A>T	NP_000558.2:n.*221A>T
XM_011509207.1:c.*22+199A>T	XP_011507509.1:n.*22+199A>T
NM_001329057.1:c.*22+199A>T	NP_001315986.1:n.*22+199A>T
NM_001329058.1:c.*22+199A>T	NP_001315987.1:n.*22+199A>T
NM_000567.3:c.*221A>T MANE Select	NP_000558.2:n.*221A>T
NM_001329057.2:c.*22+199A>T	NP_001315986.1:n.*22+199A>T
NM_001329058.2:c.*22+199A>T	NP_001315987.1:n.*22+199A>T
NM_001382703.1:c.*221A>T	NP_001369632.1:n.*221A>T