Canonical Allele Identifier: CA343453422

Gene: CRP

Linked Data

• MyVariant Identifiers: chr1:g.159683335T>A (hg19) ; chr1:g.159713545T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713545T>A , CM000663.2:g.159713545T>A	GRCh38
NC_000001.10:g.159683335T>A , CM000663.1:g.159683335T>A	GRCh37
NC_000001.9:g.157949959T>A	NCBI36
NG_013007.1:g.6045A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.655A>T MANE Select	ENSP00000255030.5:p.Lys219Ter
ENST00000368110.1:c.289A>T	ENSP00000357091.1:p.Lys97Ter
ENST00000368111.5:c.289A>T	ENSP00000357092.1:p.Lys97Ter
ENST00000368112.5:c.256A>T	ENSP00000357093.1:p.Lys86Ter
ENST00000437342.1:c.121A>T	ENSP00000402788.1:p.Lys41Ter
ENST00000473196.1:n.223A>T
ENST00000489317.1:n.74+462A>T
NM_000567.2:c.655A>T	NP_000558.2:p.Lys219Ter
XM_011509207.1:c.655A>T	XP_011507509.1:p.Lys219Ter
NM_001329057.1:c.655A>T	NP_001315986.1:p.Lys219Ter
NM_001329058.1:c.256A>T	NP_001315987.1:p.Lys86Ter
NM_000567.3:c.655A>T MANE Select	NP_000558.2:p.Lys219Ter
NM_001329057.2:c.655A>T	NP_001315986.1:p.Lys219Ter
NM_001329058.2:c.256A>T	NP_001315987.1:p.Lys86Ter
NM_001382703.1:c.289A>T	NP_001369632.1:p.Lys97Ter