Canonical Allele Identifier: CA526679662

Gene: CRP

Linked Data

• dbSNP Id: rs1557844115
• gnomAD v2: 1-159683195-CCCAGAGACAGAGACGTGGGAACCATGCAGTGTAAAAAAGCGGGAGGTA-C
• gnomAD v3: 1-159713405-CCCAGAGACAGAGACGTGGGAACCATGCAGTGTAAAAAAGCGGGAGGTA-C
• gnomAD v4: 1-159713405-CCCAGAGACAGAGACGTGGGAACCATGCAGTGTAAAAAAGCGGGAGGTA-C
• MyVariant Identifiers: chr1:g.159683196_159683243del (hg19) ; chr1:g.159713406_159713453del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713425_159713472del , CM000663.2:g.159713425_159713472del	GRCh38
NC_000001.10:g.159683215_159683262del , CM000663.1:g.159683215_159683262del	GRCh37
NC_000001.9:g.157949839_157949886del	NCBI36
NG_013007.1:g.6137_6184del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*72_*119del MANE Select	ENSP00000255030.5:n.*72_*119del
ENST00000368110.1:c.*22+50_*22+97del	ENSP00000357091.1:n.*22+50_*22+97del
ENST00000368111.5:c.*22+50_*22+97del	ENSP00000357092.1:n.*22+50_*22+97del
ENST00000368112.5:c.*22+50_*22+97del	ENSP00000357093.1:n.*22+50_*22+97del
ENST00000437342.1:c.*22+50_*22+97del	ENSP00000402788.1:n.*22+50_*22+97del
ENST00000473196.1:n.265+50_265+97del
ENST00000489317.1:n.74+554_74+601del
NM_000567.2:c.*72_*119del	NP_000558.2:n.*72_*119del
XM_011509207.1:c.*22+50_*22+97del	XP_011507509.1:n.*22+50_*22+97del
NM_001329057.1:c.*22+50_*22+97del	NP_001315986.1:n.*22+50_*22+97del
NM_001329058.1:c.*22+50_*22+97del	NP_001315987.1:n.*22+50_*22+97del
NM_000567.3:c.*72_*119del MANE Select	NP_000558.2:n.*72_*119del
NM_001329057.2:c.*22+50_*22+97del	NP_001315986.1:n.*22+50_*22+97del
NM_001329058.2:c.*22+50_*22+97del	NP_001315987.1:n.*22+50_*22+97del
NM_001382703.1:c.*72_*119del	NP_001369632.1:n.*72_*119del