Canonical Allele Identifier: CA1202014903
Gene: CRP HGNC NCBI

Linked Data

dbSNP Id: rs1660714996

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159713063_159713064insTGATT , CM000663.2:g.159713063_159713064insTGATT GRCh38
NC_000001.10:g.159682853_159682854insTGATT , CM000663.1:g.159682853_159682854insTGATT GRCh37
NC_000001.9:g.157949477_157949478insTGATT NCBI36
NG_013007.1:g.6526_6527insAATCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000255030.9:c.*461_*462insAATCA MANE Select ENSP00000255030.5:n.*461_*462insAATCA
ENST00000368110.1:c.*23-270_*23-269insAATCA ENSP00000357091.1:n.*23-270_*23-269insAATCA
ENST00000368111.5:c.*22+439_*22+440insAATCA ENSP00000357092.1:n.*22+439_*22+440insAATCA
ENST00000368112.5:c.*23-270_*23-269insAATCA ENSP00000357093.1:n.*23-270_*23-269insAATCA
ENST00000437342.1:c.*23-270_*23-269insAATCA ENSP00000402788.1:n.*23-270_*23-269insAATCA
ENST00000473196.1:n.266-270_266-269insAATCA
ENST00000489317.1:n.75-270_75-269insAATCA
NM_000567.2:c.*461_*462insAATCA NP_000558.2:n.*461_*462insAATCA
XM_011509207.1:c.*23-270_*23-269insAATCA XP_011507509.1:n.*23-270_*23-269insAATCA
NM_001329057.1:c.*23-270_*23-269insAATCA NP_001315986.1:n.*23-270_*23-269insAATCA
NM_001329058.1:c.*22+439_*22+440insAATCA NP_001315987.1:n.*22+439_*22+440insAATCA
NM_000567.3:c.*461_*462insAATCA MANE Select NP_000558.2:n.*461_*462insAATCA
NM_001329057.2:c.*23-270_*23-269insAATCA NP_001315986.1:n.*23-270_*23-269insAATCA
NM_001329058.2:c.*22+439_*22+440insAATCA NP_001315987.1:n.*22+439_*22+440insAATCA
NM_001382703.1:c.*461_*462insAATCA NP_001369632.1:n.*461_*462insAATCA