Canonical Allele Identifier: CA343454276

Gene: CRP

Linked Data

• MyVariant Identifiers: chr1:g.159683629C>A (hg19) ; chr1:g.159713839C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713839C>A , CM000663.2:g.159713839C>A	GRCh38
NC_000001.10:g.159683629C>A , CM000663.1:g.159683629C>A	GRCh37
NC_000001.9:g.157950253C>A	NCBI36
NG_013007.1:g.5751G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.361G>T MANE Select	ENSP00000255030.5:p.Ala121Ser
ENST00000368110.1:c.193+168G>T	ENSP00000357091.1:n.193+168G>T
ENST00000368111.5:c.193+168G>T	ENSP00000357092.1:n.193+168G>T
ENST00000368112.5:c.197+164G>T	ENSP00000357093.1:n.197+164G>T
ENST00000437342.1:c.-174G>T	ENSP00000402788.1:n.-174G>T
ENST00000489317.1:n.74+168G>T
NM_000567.2:c.361G>T	NP_000558.2:p.Ala121Ser
XM_011509207.1:c.361G>T	XP_011507509.1:p.Ala121Ser
NM_001329057.1:c.361G>T	NP_001315986.1:p.Ala121Ser
NM_001329058.1:c.197+164G>T	NP_001315987.1:n.197+164G>T
NM_000567.3:c.361G>T MANE Select	NP_000558.2:p.Ala121Ser
NM_001329057.2:c.361G>T	NP_001315986.1:p.Ala121Ser
NM_001329058.2:c.197+164G>T	NP_001315987.1:n.197+164G>T
NM_001382703.1:c.193+168G>T	NP_001369632.1:n.193+168G>T