Canonical Allele Identifier: CA1202014757

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712914_159712915delinsCT , CM000663.2:g.159712914_159712915delinsCT	GRCh38
NC_000001.10:g.159682704_159682705delinsCT , CM000663.1:g.159682704_159682705delinsCT	GRCh37
NC_000001.9:g.157949328_157949329delinsCT	NCBI36
NG_013007.1:g.6675_6676delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*610_*611delinsAG MANE Select	ENSP00000255030.5:n.*610_*611delinsAG
ENST00000368110.1:c.*23-121_*23-120delinsAG	ENSP00000357091.1:n.*23-121_*23-120delinsAG
ENST00000368111.5:c.*23-335_*23-334delinsAG	ENSP00000357092.1:n.*23-335_*23-334delinsAG
ENST00000368112.5:c.*23-121_*23-120delinsAG	ENSP00000357093.1:n.*23-121_*23-120delinsAG
ENST00000437342.1:c.*23-121_*23-120delinsAG	ENSP00000402788.1:n.*23-121_*23-120delinsAG
ENST00000473196.1:n.266-121_266-120delinsAG
ENST00000489317.1:n.75-121_75-120delinsAG
NM_000567.2:c.*610_*611delinsAG	NP_000558.2:n.*610_*611delinsAG
XM_011509207.1:c.*23-121_*23-120delinsAG	XP_011507509.1:n.*23-121_*23-120delinsAG
NM_001329057.1:c.*23-121_*23-120delinsAG	NP_001315986.1:n.*23-121_*23-120delinsAG
NM_001329058.1:c.*23-347_*23-346delinsAG	NP_001315987.1:n.*23-347_*23-346delinsAG
NM_000567.3:c.*610_*611delinsAG MANE Select	NP_000558.2:n.*610_*611delinsAG
NM_001329057.2:c.*23-121_*23-120delinsAG	NP_001315986.1:n.*23-121_*23-120delinsAG
NM_001329058.2:c.*23-347_*23-346delinsAG	NP_001315987.1:n.*23-347_*23-346delinsAG
NM_001382703.1:c.*610_*611delinsAG	NP_001369632.1:n.*610_*611delinsAG