Canonical Allele Identifier: CA1144911036

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712874_159712880delinsAAAAAAA , CM000663.2:g.159712874_159712880delinsAAAAAAA	GRCh38
NC_000001.10:g.159682664_159682670delinsAAAAAAA , CM000663.1:g.159682664_159682670delinsAAAAAAA	GRCh37
NC_000001.9:g.157949288_157949294delinsAAAAAAA	NCBI36
NG_013007.1:g.6710_6716delinsTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*645_*651delinsTTTTTTT MANE Select	ENSP00000255030.5:n.*645_*651delinsTTTTTTT
ENST00000368110.1:c.*23-86_*23-80delinsTTTTTTT	ENSP00000357091.1:n.*23-86_*23-80delinsTTTTTTT
ENST00000368111.5:c.*23-300_*23-294delinsTTTTTTT	ENSP00000357092.1:n.*23-300_*23-294delinsTTTTTTT
ENST00000368112.5:c.*23-86_*23-80delinsTTTTTTT	ENSP00000357093.1:n.*23-86_*23-80delinsTTTTTTT
ENST00000437342.1:c.*23-86_*23-80delinsTTTTTTT	ENSP00000402788.1:n.*23-86_*23-80delinsTTTTTTT
ENST00000473196.1:n.266-86_266-80delinsTTTTTTT
ENST00000489317.1:n.75-86_75-80delinsTTTTTTT
NM_000567.2:c.*645_*651delinsTTTTTTT	NP_000558.2:n.*645_*651delinsTTTTTTT
XM_011509207.1:c.*23-86_*23-80delinsTTTTTTT	XP_011507509.1:n.*23-86_*23-80delinsTTTTTTT
NM_001329057.1:c.*23-86_*23-80delinsTTTTTTT	NP_001315986.1:n.*23-86_*23-80delinsTTTTTTT
NM_001329058.1:c.*23-312_*23-306delinsTTTTTTT	NP_001315987.1:n.*23-312_*23-306delinsTTTTTTT
NM_000567.3:c.*645_*651delinsTTTTTTT MANE Select	NP_000558.2:n.*645_*651delinsTTTTTTT
NM_001329057.2:c.*23-86_*23-80delinsTTTTTTT	NP_001315986.1:n.*23-86_*23-80delinsTTTTTTT
NM_001329058.2:c.*23-312_*23-306delinsTTTTTTT	NP_001315987.1:n.*23-312_*23-306delinsTTTTTTT
NM_001382703.1:c.*645_*651delinsTTTTTTT	NP_001369632.1:n.*645_*651delinsTTTTTTT