Canonical Allele Identifier: CA421618503

Gene: CRP

Linked Data

• dbSNP Id: rs1660741141
• MyVariant Identifiers: chr1:g.159683531C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713741C>T , CM000663.2:g.159713741C>T	GRCh38
NC_000001.10:g.159683531C>T , CM000663.1:g.159683531C>T	GRCh37
NC_000001.9:g.157950155C>T	NCBI36
NG_013007.1:g.5849G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.459G>A MANE Select	ENSP00000255030.5:p.Leu153=
ENST00000368110.1:c.194-101G>A	ENSP00000357091.1:n.194-101G>A
ENST00000368111.5:c.194-101G>A	ENSP00000357092.1:n.194-101G>A
ENST00000368112.5:c.198-138G>A	ENSP00000357093.1:n.198-138G>A
ENST00000437342.1:c.-76G>A	ENSP00000402788.1:n.-76G>A
ENST00000473196.1:n.27G>A
ENST00000489317.1:n.74+266G>A
NM_000567.2:c.459G>A	NP_000558.2:p.Leu153=
XM_011509207.1:c.459G>A	XP_011507509.1:p.Leu153=
NM_001329057.1:c.459G>A	NP_001315986.1:p.Leu153=
NM_001329058.1:c.198-138G>A	NP_001315987.1:n.198-138G>A
NM_000567.3:c.459G>A MANE Select	NP_000558.2:p.Leu153=
NM_001329057.2:c.459G>A	NP_001315986.1:p.Leu153=
NM_001329058.2:c.198-138G>A	NP_001315987.1:n.198-138G>A
NM_001382703.1:c.194-101G>A	NP_001369632.1:n.194-101G>A