Canonical Allele Identifier: CA1202014306

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712466_159712468delinsAAG , CM000663.2:g.159712466_159712468delinsAAG	GRCh38
NC_000001.10:g.159682256_159682258delinsAAG , CM000663.1:g.159682256_159682258delinsAAG	GRCh37
NC_000001.9:g.157948880_157948882delinsAAG	NCBI36
NG_013007.1:g.7122_7124delinsCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*1057_*1059delinsCTT MANE Select	ENSP00000255030.5:n.*1057_*1059delinsCTT
ENST00000368112.5:c.*349_*351delinsCTT	ENSP00000357093.1:n.*349_*351delinsCTT
ENST00000437342.1:c.*349_*351delinsCTT	ENSP00000402788.1:n.*349_*351delinsCTT
ENST00000473196.1:n.592_594delinsCTT
NM_000567.2:c.*1057_*1059delinsCTT	NP_000558.2:n.*1057_*1059delinsCTT
XM_011509207.1:c.*349_*351delinsCTT	XP_011507509.1:n.*349_*351delinsCTT
NM_001329057.1:c.*349_*351delinsCTT	NP_001315986.1:n.*349_*351delinsCTT
NM_001329058.1:c.*123_*125delinsCTT	NP_001315987.1:n.*123_*125delinsCTT
NM_000567.3:c.*1057_*1059delinsCTT MANE Select	NP_000558.2:n.*1057_*1059delinsCTT
NM_001329057.2:c.*349_*351delinsCTT	NP_001315986.1:n.*349_*351delinsCTT
NM_001329058.2:c.*123_*125delinsCTT	NP_001315987.1:n.*123_*125delinsCTT
NM_001382703.1:c.*1057_*1059delinsCTT	NP_001369632.1:n.*1057_*1059delinsCTT