Canonical Allele Identifier: CA343453455

Gene: CRP

Linked Data

• gnomAD v4: 1-159713560-C-T
• MyVariant Identifiers: chr1:g.159683350C>T (hg19) ; chr1:g.159713560C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713560C>T , CM000663.2:g.159713560C>T	GRCh38
NC_000001.10:g.159683350C>T , CM000663.1:g.159683350C>T	GRCh37
NC_000001.9:g.157949974C>T	NCBI36
NG_013007.1:g.6030G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.640G>A MANE Select	ENSP00000255030.5:p.Gly214Ser
ENST00000368110.1:c.274G>A	ENSP00000357091.1:p.Gly92Ser
ENST00000368111.5:c.274G>A	ENSP00000357092.1:p.Gly92Ser
ENST00000368112.5:c.241G>A	ENSP00000357093.1:p.Gly81Ser
ENST00000437342.1:c.106G>A	ENSP00000402788.1:p.Gly36Ser
ENST00000473196.1:n.208G>A
ENST00000489317.1:n.74+447G>A
NM_000567.2:c.640G>A	NP_000558.2:p.Gly214Ser
XM_011509207.1:c.640G>A	XP_011507509.1:p.Gly214Ser
NM_001329057.1:c.640G>A	NP_001315986.1:p.Gly214Ser
NM_001329058.1:c.241G>A	NP_001315987.1:p.Gly81Ser
NM_000567.3:c.640G>A MANE Select	NP_000558.2:p.Gly214Ser
NM_001329057.2:c.640G>A	NP_001315986.1:p.Gly214Ser
NM_001329058.2:c.241G>A	NP_001315987.1:p.Gly81Ser
NM_001382703.1:c.274G>A	NP_001369632.1:p.Gly92Ser