Canonical Allele Identifier: CA526679667

Gene: CRP

Linked Data

• dbSNP Id: rs1369901370
• gnomAD v2: 1-159683227-T-TA
• gnomAD v3: 1-159713437-T-TA
• gnomAD v4: 1-159713437-T-TA
• MyVariant Identifiers: chr1:g.159683227_159683228insA (hg19) ; chr1:g.159713437_159713438insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713443dup , CM000663.2:g.159713443dup	GRCh38
NC_000001.10:g.159683233dup , CM000663.1:g.159683233dup	GRCh37
NC_000001.9:g.157949857dup	NCBI36
NG_013007.1:g.6152dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*87dup MANE Select	ENSP00000255030.5:n.*87dup
ENST00000368110.1:c.*22+65dup	ENSP00000357091.1:n.*22+65dup
ENST00000368111.5:c.*22+65dup	ENSP00000357092.1:n.*22+65dup
ENST00000368112.5:c.*22+65dup	ENSP00000357093.1:n.*22+65dup
ENST00000437342.1:c.*22+65dup	ENSP00000402788.1:n.*22+65dup
ENST00000473196.1:n.265+65dup
ENST00000489317.1:n.74+569dup
NM_000567.2:c.*87dup	NP_000558.2:n.*87dup
XM_011509207.1:c.*22+65dup	XP_011507509.1:n.*22+65dup
NM_001329057.1:c.*22+65dup	NP_001315986.1:n.*22+65dup
NM_001329058.1:c.*22+65dup	NP_001315987.1:n.*22+65dup
NM_000567.3:c.*87dup MANE Select	NP_000558.2:n.*87dup
NM_001329057.2:c.*22+65dup	NP_001315986.1:n.*22+65dup
NM_001329058.2:c.*22+65dup	NP_001315987.1:n.*22+65dup
NM_001382703.1:c.*87dup	NP_001369632.1:n.*87dup