Canonical Allele Identifier: CA1202015084

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713314_159713315delinsGT , CM000663.2:g.159713314_159713315delinsGT	GRCh38
NC_000001.10:g.159683104_159683105delinsGT , CM000663.1:g.159683104_159683105delinsGT	GRCh37
NC_000001.9:g.157949728_157949729delinsGT	NCBI36
NG_013007.1:g.6275_6276delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*210_*211delinsAC MANE Select	ENSP00000255030.5:n.*210_*211delinsAC
ENST00000368110.1:c.*22+188_*22+189delinsAC	ENSP00000357091.1:n.*22+188_*22+189delins...
ENST00000368111.5:c.*22+188_*22+189delinsAC	ENSP00000357092.1:n.*22+188_*22+189delins...
ENST00000368112.5:c.*22+188_*22+189delinsAC	ENSP00000357093.1:n.*22+188_*22+189delins...
ENST00000437342.1:c.*22+188_*22+189delinsAC	ENSP00000402788.1:n.*22+188_*22+189delins...
ENST00000473196.1:n.265+188_265+189delinsAC
ENST00000489317.1:n.75-521_75-520delinsAC
NM_000567.2:c.*210_*211delinsAC	NP_000558.2:n.*210_*211delinsAC
XM_011509207.1:c.*22+188_*22+189delinsAC	XP_011507509.1:n.*22+188_*22+189delinsAC
NM_001329057.1:c.*22+188_*22+189delinsAC	NP_001315986.1:n.*22+188_*22+189delinsAC
NM_001329058.1:c.*22+188_*22+189delinsAC	NP_001315987.1:n.*22+188_*22+189delinsAC
NM_000567.3:c.*210_*211delinsAC MANE Select	NP_000558.2:n.*210_*211delinsAC
NM_001329057.2:c.*22+188_*22+189delinsAC	NP_001315986.1:n.*22+188_*22+189delinsAC
NM_001329058.2:c.*22+188_*22+189delinsAC	NP_001315987.1:n.*22+188_*22+189delinsAC
NM_001382703.1:c.*210_*211delinsAC	NP_001369632.1:n.*210_*211delinsAC