Canonical Allele Identifier: CA646341032

Gene: CRP

Linked Data

• COSMIC: COSN22556352

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713074_159713075insA , CM000663.2:g.159713074_159713075insA	GRCh38
NC_000001.10:g.159682864_159682865insA , CM000663.1:g.159682864_159682865insA	GRCh37
NC_000001.9:g.157949488_157949489insA	NCBI36
NG_013007.1:g.6515_6516insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*450_*451insT MANE Select	ENSP00000255030.5:n.*450_*451insT
ENST00000368110.1:c.*23-281_*23-280insT	ENSP00000357091.1:n.*23-281_*23-280insT
ENST00000368111.5:c.*22+428_*22+429insT	ENSP00000357092.1:n.*22+428_*22+429insT
ENST00000368112.5:c.*23-281_*23-280insT	ENSP00000357093.1:n.*23-281_*23-280insT
ENST00000437342.1:c.*23-281_*23-280insT	ENSP00000402788.1:n.*23-281_*23-280insT
ENST00000473196.1:n.266-281_266-280insT
ENST00000489317.1:n.75-281_75-280insT
NM_000567.2:c.*450_*451insT	NP_000558.2:n.*450_*451insT
XM_011509207.1:c.*23-281_*23-280insT	XP_011507509.1:n.*23-281_*23-280insT
NM_001329057.1:c.*23-281_*23-280insT	NP_001315986.1:n.*23-281_*23-280insT
NM_001329058.1:c.*22+428_*22+429insT	NP_001315987.1:n.*22+428_*22+429insT
NM_000567.3:c.*450_*451insT MANE Select	NP_000558.2:n.*450_*451insT
NM_001329057.2:c.*23-281_*23-280insT	NP_001315986.1:n.*23-281_*23-280insT
NM_001329058.2:c.*22+428_*22+429insT	NP_001315987.1:n.*22+428_*22+429insT
NM_001382703.1:c.*450_*451insT	NP_001369632.1:n.*450_*451insT