Canonical Allele Identifier: CA343454281

Gene: CRP

Linked Data

• MyVariant Identifiers: chr1:g.159683632A>C (hg19) ; chr1:g.159713842A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713842A>C , CM000663.2:g.159713842A>C	GRCh38
NC_000001.10:g.159683632A>C , CM000663.1:g.159683632A>C	GRCh37
NC_000001.9:g.157950256A>C	NCBI36
NG_013007.1:g.5748T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.358T>G MANE Select	ENSP00000255030.5:p.Ser120Ala
ENST00000368110.1:c.193+165T>G	ENSP00000357091.1:n.193+165T>G
ENST00000368111.5:c.193+165T>G	ENSP00000357092.1:n.193+165T>G
ENST00000368112.5:c.197+161T>G	ENSP00000357093.1:n.197+161T>G
ENST00000437342.1:c.-177T>G	ENSP00000402788.1:n.-177T>G
ENST00000489317.1:n.74+165T>G
NM_000567.2:c.358T>G	NP_000558.2:p.Ser120Ala
XM_011509207.1:c.358T>G	XP_011507509.1:p.Ser120Ala
NM_001329057.1:c.358T>G	NP_001315986.1:p.Ser120Ala
NM_001329058.1:c.197+161T>G	NP_001315987.1:n.197+161T>G
NM_000567.3:c.358T>G MANE Select	NP_000558.2:p.Ser120Ala
NM_001329057.2:c.358T>G	NP_001315986.1:p.Ser120Ala
NM_001329058.2:c.197+161T>G	NP_001315987.1:n.197+161T>G
NM_001382703.1:c.193+165T>G	NP_001369632.1:n.193+165T>G