Canonical Allele Identifier: CA1189209
Gene: CRP HGNC NCBI

Linked Data

dbSNP Id: rs773785783

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159713899_159713901del , CM000663.2:g.159713899_159713901del GRCh38
NC_000001.10:g.159683689_159683691del , CM000663.1:g.159683689_159683691del GRCh37
NC_000001.9:g.157950313_157950315del NCBI36
NG_013007.1:g.5693_5695del

Transcript Alleles

HGVS Amino-acid Change
ENST00000255030.9:c.303_305del MANE Select ENSP00000255030.5:p.Leu101del
ENST00000368110.1:c.193+110_193+112del ENSP00000357091.1:n.193+110_193+112del
ENST00000368111.5:c.193+110_193+112del ENSP00000357092.1:n.193+110_193+112del
ENST00000368112.5:c.197+106_197+108del ENSP00000357093.1:n.197+106_197+108del
ENST00000437342.1:c.-232_-230del ENSP00000402788.1:n.-232_-230del
ENST00000489317.1:n.74+110_74+112del
NM_000567.2:c.303_305del NP_000558.2:p.Leu101del
XM_011509207.1:c.303_305del XP_011507509.1:p.Leu101del
NM_001329057.1:c.303_305del NP_001315986.1:p.Leu101del
NM_001329058.1:c.197+106_197+108del NP_001315987.1:n.197+106_197+108del
NM_000567.3:c.303_305del MANE Select NP_000558.2:p.Leu101del
NM_001329057.2:c.303_305del NP_001315986.1:p.Leu101del
NM_001329058.2:c.197+106_197+108del NP_001315987.1:n.197+106_197+108del
NM_001382703.1:c.193+110_193+112del NP_001369632.1:n.193+110_193+112del