Canonical Allele Identifier: CA1202014999

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713166_159713167delinsGT , CM000663.2:g.159713166_159713167delinsGT	GRCh38
NC_000001.10:g.159682956_159682957delinsGT , CM000663.1:g.159682956_159682957delinsGT	GRCh37
NC_000001.9:g.157949580_157949581delinsGT	NCBI36
NG_013007.1:g.6423_6424delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*358_*359delinsAC MANE Select	ENSP00000255030.5:n.*358_*359delinsAC
ENST00000368110.1:c.*22+336_*22+337delinsAC	ENSP00000357091.1:n.*22+336_*22+337delinsAC
ENST00000368111.5:c.*22+336_*22+337delinsAC	ENSP00000357092.1:n.*22+336_*22+337delinsAC
ENST00000368112.5:c.*22+336_*22+337delinsAC	ENSP00000357093.1:n.*22+336_*22+337delinsAC
ENST00000437342.1:c.*22+336_*22+337delinsAC	ENSP00000402788.1:n.*22+336_*22+337delinsAC
ENST00000473196.1:n.265+336_265+337delinsAC
ENST00000489317.1:n.75-373_75-372delinsAC
NM_000567.2:c.*358_*359delinsAC	NP_000558.2:n.*358_*359delinsAC
XM_011509207.1:c.*22+336_*22+337delinsAC	XP_011507509.1:n.*22+336_*22+337delinsAC
NM_001329057.1:c.*22+336_*22+337delinsAC	NP_001315986.1:n.*22+336_*22+337delinsAC
NM_001329058.1:c.*22+336_*22+337delinsAC	NP_001315987.1:n.*22+336_*22+337delinsAC
NM_000567.3:c.*358_*359delinsAC MANE Select	NP_000558.2:n.*358_*359delinsAC
NM_001329057.2:c.*22+336_*22+337delinsAC	NP_001315986.1:n.*22+336_*22+337delinsAC
NM_001329058.2:c.*22+336_*22+337delinsAC	NP_001315987.1:n.*22+336_*22+337delinsAC
NM_001382703.1:c.*358_*359delinsAC	NP_001369632.1:n.*358_*359delinsAC