Canonical Allele Identifier: CA421618652

Gene: CRP

Linked Data

• MyVariant Identifiers: chr1:g.159683642T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713852T>G , CM000663.2:g.159713852T>G	GRCh38
NC_000001.10:g.159683642T>G , CM000663.1:g.159683642T>G	GRCh37
NC_000001.9:g.157950266T>G	NCBI36
NG_013007.1:g.5738A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.348A>C MANE Select	ENSP00000255030.5:p.Thr116=
ENST00000368110.1:c.193+155A>C	ENSP00000357091.1:n.193+155A>C
ENST00000368111.5:c.193+155A>C	ENSP00000357092.1:n.193+155A>C
ENST00000368112.5:c.197+151A>C	ENSP00000357093.1:n.197+151A>C
ENST00000437342.1:c.-187A>C	ENSP00000402788.1:n.-187A>C
ENST00000489317.1:n.74+155A>C
NM_000567.2:c.348A>C	NP_000558.2:p.Thr116=
XM_011509207.1:c.348A>C	XP_011507509.1:p.Thr116=
NM_001329057.1:c.348A>C	NP_001315986.1:p.Thr116=
NM_001329058.1:c.197+151A>C	NP_001315987.1:n.197+151A>C
NM_000567.3:c.348A>C MANE Select	NP_000558.2:p.Thr116=
NM_001329057.2:c.348A>C	NP_001315986.1:p.Thr116=
NM_001329058.2:c.197+151A>C	NP_001315987.1:n.197+151A>C
NM_001382703.1:c.193+155A>C	NP_001369632.1:n.193+155A>C