Canonical Allele Identifier: CA343454162

Gene: CRP

Linked Data

• gnomAD v4: 1-159713785-G-C
• MyVariant Identifiers: chr1:g.159683575G>C (hg19) ; chr1:g.159713785G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713785G>C , CM000663.2:g.159713785G>C	GRCh38
NC_000001.10:g.159683575G>C , CM000663.1:g.159683575G>C	GRCh37
NC_000001.9:g.157950199G>C	NCBI36
NG_013007.1:g.5805C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.415C>G MANE Select	ENSP00000255030.5:p.Leu139Val
ENST00000368110.1:c.194-145C>G	ENSP00000357091.1:n.194-145C>G
ENST00000368111.5:c.194-145C>G	ENSP00000357092.1:n.194-145C>G
ENST00000368112.5:c.198-182C>G	ENSP00000357093.1:n.198-182C>G
ENST00000437342.1:c.-120C>G	ENSP00000402788.1:n.-120C>G
ENST00000489317.1:n.74+222C>G
NM_000567.2:c.415C>G	NP_000558.2:p.Leu139Val
XM_011509207.1:c.415C>G	XP_011507509.1:p.Leu139Val
NM_001329057.1:c.415C>G	NP_001315986.1:p.Leu139Val
NM_001329058.1:c.198-182C>G	NP_001315987.1:n.198-182C>G
NM_000567.3:c.415C>G MANE Select	NP_000558.2:p.Leu139Val
NM_001329057.2:c.415C>G	NP_001315986.1:p.Leu139Val
NM_001329058.2:c.198-182C>G	NP_001315987.1:n.198-182C>G
NM_001382703.1:c.194-145C>G	NP_001369632.1:n.194-145C>G