Canonical Allele Identifier: CA1202014697

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712873_159712874delinsGA , CM000663.2:g.159712873_159712874delinsGA	GRCh38
NC_000001.10:g.159682663_159682664delinsGA , CM000663.1:g.159682663_159682664delinsGA	GRCh37
NC_000001.9:g.157949287_157949288delinsGA	NCBI36
NG_013007.1:g.6716_6717delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*651_*652delinsTC MANE Select	ENSP00000255030.5:n.*651_*652delinsTC
ENST00000368110.1:c.*23-80_*23-79delinsTC	ENSP00000357091.1:n.*23-80_*23-79delinsTC
ENST00000368111.5:c.*23-294_*23-293delinsTC	ENSP00000357092.1:n.*23-294_*23-293delinsTC
ENST00000368112.5:c.*23-80_*23-79delinsTC	ENSP00000357093.1:n.*23-80_*23-79delinsTC
ENST00000437342.1:c.*23-80_*23-79delinsTC	ENSP00000402788.1:n.*23-80_*23-79delinsTC
ENST00000473196.1:n.266-80_266-79delinsTC
ENST00000489317.1:n.75-80_75-79delinsTC
NM_000567.2:c.*651_*652delinsTC	NP_000558.2:n.*651_*652delinsTC
XM_011509207.1:c.*23-80_*23-79delinsTC	XP_011507509.1:n.*23-80_*23-79delinsTC
NM_001329057.1:c.*23-80_*23-79delinsTC	NP_001315986.1:n.*23-80_*23-79delinsTC
NM_001329058.1:c.*23-306_*23-305delinsTC	NP_001315987.1:n.*23-306_*23-305delinsTC
NM_000567.3:c.*651_*652delinsTC MANE Select	NP_000558.2:n.*651_*652delinsTC
NM_001329057.2:c.*23-80_*23-79delinsTC	NP_001315986.1:n.*23-80_*23-79delinsTC
NM_001329058.2:c.*23-306_*23-305delinsTC	NP_001315987.1:n.*23-306_*23-305delinsTC
NM_001382703.1:c.*651_*652delinsTC	NP_001369632.1:n.*651_*652delinsTC