Canonical Allele Identifier: CA343454139

Gene: CRP

Linked Data

• gnomAD v4: 1-159713775-C-A
• MyVariant Identifiers: chr1:g.159683565C>A (hg19) ; chr1:g.159713775C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713775C>A , CM000663.2:g.159713775C>A	GRCh38
NC_000001.10:g.159683565C>A , CM000663.1:g.159683565C>A	GRCh37
NC_000001.9:g.157950189C>A	NCBI36
NG_013007.1:g.5815G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.425G>T MANE Select	ENSP00000255030.5:p.Gly142Val
ENST00000368110.1:c.194-135G>T	ENSP00000357091.1:n.194-135G>T
ENST00000368111.5:c.194-135G>T	ENSP00000357092.1:n.194-135G>T
ENST00000368112.5:c.198-172G>T	ENSP00000357093.1:n.198-172G>T
ENST00000437342.1:c.-110G>T	ENSP00000402788.1:n.-110G>T
ENST00000489317.1:n.74+232G>T
NM_000567.2:c.425G>T	NP_000558.2:p.Gly142Val
XM_011509207.1:c.425G>T	XP_011507509.1:p.Gly142Val
NM_001329057.1:c.425G>T	NP_001315986.1:p.Gly142Val
NM_001329058.1:c.198-172G>T	NP_001315987.1:n.198-172G>T
NM_000567.3:c.425G>T MANE Select	NP_000558.2:p.Gly142Val
NM_001329057.2:c.425G>T	NP_001315986.1:p.Gly142Val
NM_001329058.2:c.198-172G>T	NP_001315987.1:n.198-172G>T
NM_001382703.1:c.194-135G>T	NP_001369632.1:n.194-135G>T