Canonical Allele Identifier: CA2648593403

Gene: CRP

Linked Data

• gnomAD v4: 1-159713253-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713256del , CM000663.2:g.159713256del	GRCh38
NC_000001.10:g.159683046del , CM000663.1:g.159683046del	GRCh37
NC_000001.9:g.157949670del	NCBI36
NG_013007.1:g.6336del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*271del MANE Select	ENSP00000255030.5:n.*271del
ENST00000368110.1:c.*22+249del	ENSP00000357091.1:n.*22+249del
ENST00000368111.5:c.*22+249del	ENSP00000357092.1:n.*22+249del
ENST00000368112.5:c.*22+249del	ENSP00000357093.1:n.*22+249del
ENST00000437342.1:c.*22+249del	ENSP00000402788.1:n.*22+249del
ENST00000473196.1:n.265+249del
ENST00000489317.1:n.75-460del
NM_000567.2:c.*271del	NP_000558.2:n.*271del
XM_011509207.1:c.*22+249del	XP_011507509.1:n.*22+249del
NM_001329057.1:c.*22+249del	NP_001315986.1:n.*22+249del
NM_001329058.1:c.*22+249del	NP_001315987.1:n.*22+249del
NM_000567.3:c.*271del MANE Select	NP_000558.2:n.*271del
NM_001329057.2:c.*22+249del	NP_001315986.1:n.*22+249del
NM_001329058.2:c.*22+249del	NP_001315987.1:n.*22+249del
NM_001382703.1:c.*271del	NP_001369632.1:n.*271del