Canonical Allele Identifier: CA343454207

Gene: CRP

Linked Data

• MyVariant Identifiers: chr1:g.159683595T>G (hg19) ; chr1:g.159713805T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713805T>G , CM000663.2:g.159713805T>G	GRCh38
NC_000001.10:g.159683595T>G , CM000663.1:g.159683595T>G	GRCh37
NC_000001.9:g.157950219T>G	NCBI36
NG_013007.1:g.5785A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.395A>C MANE Select	ENSP00000255030.5:p.Lys132Thr
ENST00000368110.1:c.194-165A>C	ENSP00000357091.1:n.194-165A>C
ENST00000368111.5:c.194-165A>C	ENSP00000357092.1:n.194-165A>C
ENST00000368112.5:c.197+198A>C	ENSP00000357093.1:n.197+198A>C
ENST00000437342.1:c.-140A>C	ENSP00000402788.1:n.-140A>C
ENST00000489317.1:n.74+202A>C
NM_000567.2:c.395A>C	NP_000558.2:p.Lys132Thr
XM_011509207.1:c.395A>C	XP_011507509.1:p.Lys132Thr
NM_001329057.1:c.395A>C	NP_001315986.1:p.Lys132Thr
NM_001329058.1:c.197+198A>C	NP_001315987.1:n.197+198A>C
NM_000567.3:c.395A>C MANE Select	NP_000558.2:p.Lys132Thr
NM_001329057.2:c.395A>C	NP_001315986.1:p.Lys132Thr
NM_001329058.2:c.197+198A>C	NP_001315987.1:n.197+198A>C
NM_001382703.1:c.194-165A>C	NP_001369632.1:n.194-165A>C