Canonical Allele Identifier: CA1008297652
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712348_159712350del , CM000663.2:g.159712348_159712350del GRCh38
NC_000001.10:g.159682138_159682140del , CM000663.1:g.159682138_159682140del GRCh37
NC_000001.9:g.157948762_157948764del NCBI36
NG_013007.1:g.7240_7242del

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1175_*1177del MANE Select ENSP00000255030.5:n.*1175_*1177del
ENST00000437342.1:c.*467_*469del ENSP00000402788.1:n.*467_*469del
ENST00000473196.1:n.710_712del
NM_000567.2:c.*1175_*1177del NP_000558.2:n.*1175_*1177del
XM_011509207.1:c.*467_*469del XP_011507509.1:n.*467_*469del
NM_001329057.1:c.*467_*469del NP_001315986.1:n.*467_*469del
NM_001329058.1:c.*241_*243del NP_001315987.1:n.*241_*243del
NM_000567.3:c.*1175_*1177del MANE Select NP_000558.2:n.*1175_*1177del
NM_001329057.2:c.*467_*469del NP_001315986.1:n.*467_*469del
NM_001329058.2:c.*241_*243del NP_001315987.1:n.*241_*243del
NM_001382703.1:c.*1175_*1177del NP_001369632.1:n.*1175_*1177del