Canonical Allele Identifier: CA1202014946

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713102_159713103delinsTG , CM000663.2:g.159713102_159713103delinsTG	GRCh38
NC_000001.10:g.159682892_159682893delinsTG , CM000663.1:g.159682892_159682893delinsTG	GRCh37
NC_000001.9:g.157949516_157949517delinsTG	NCBI36
NG_013007.1:g.6487_6488delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*422_*423delinsCA MANE Select	ENSP00000255030.5:n.*422_*423delinsCA
ENST00000368110.1:c.*23-309_*23-308delinsCA	ENSP00000357091.1:n.*23-309_*23-308delinsCA
ENST00000368111.5:c.*22+400_*22+401delinsCA	ENSP00000357092.1:n.*22+400_*22+401delinsCA
ENST00000368112.5:c.*23-309_*23-308delinsCA	ENSP00000357093.1:n.*23-309_*23-308delinsCA
ENST00000437342.1:c.*23-309_*23-308delinsCA	ENSP00000402788.1:n.*23-309_*23-308delinsCA
ENST00000473196.1:n.266-309_266-308delinsCA
ENST00000489317.1:n.75-309_75-308delinsCA
NM_000567.2:c.*422_*423delinsCA	NP_000558.2:n.*422_*423delinsCA
XM_011509207.1:c.*23-309_*23-308delinsCA	XP_011507509.1:n.*23-309_*23-308delinsCA
NM_001329057.1:c.*23-309_*23-308delinsCA	NP_001315986.1:n.*23-309_*23-308delinsCA
NM_001329058.1:c.*22+400_*22+401delinsCA	NP_001315987.1:n.*22+400_*22+401delinsCA
NM_000567.3:c.*422_*423delinsCA MANE Select	NP_000558.2:n.*422_*423delinsCA
NM_001329057.2:c.*23-309_*23-308delinsCA	NP_001315986.1:n.*23-309_*23-308delinsCA
NM_001329058.2:c.*22+400_*22+401delinsCA	NP_001315987.1:n.*22+400_*22+401delinsCA
NM_001382703.1:c.*422_*423delinsCA	NP_001369632.1:n.*422_*423delinsCA