Canonical Allele Identifier: CA2648592760

Gene: CRP

Linked Data

• gnomAD v4: 1-159712357-GGCTGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712358_159712362del , CM000663.2:g.159712358_159712362del	GRCh38
NC_000001.10:g.159682148_159682152del , CM000663.1:g.159682148_159682152del	GRCh37
NC_000001.9:g.157948772_157948776del	NCBI36
NG_013007.1:g.7228_7232del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*1163_*1167del MANE Select	ENSP00000255030.5:n.*1163_*1167del
ENST00000437342.1:c.*455_*459del	ENSP00000402788.1:n.*455_*459del
ENST00000473196.1:n.698_702del
NM_000567.2:c.*1163_*1167del	NP_000558.2:n.*1163_*1167del
XM_011509207.1:c.*455_*459del	XP_011507509.1:n.*455_*459del
NM_001329057.1:c.*455_*459del	NP_001315986.1:n.*455_*459del
NM_001329058.1:c.*229_*233del	NP_001315987.1:n.*229_*233del
NM_000567.3:c.*1163_*1167del MANE Select	NP_000558.2:n.*1163_*1167del
NM_001329057.2:c.*455_*459del	NP_001315986.1:n.*455_*459del
NM_001329058.2:c.*229_*233del	NP_001315987.1:n.*229_*233del
NM_001382703.1:c.*1163_*1167del	NP_001369632.1:n.*1163_*1167del