Canonical Allele Identifier: CA421618631

Gene: CRP

Linked Data

• MyVariant Identifiers: chr1:g.159683624T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713834T>A , CM000663.2:g.159713834T>A	GRCh38
NC_000001.10:g.159683624T>A , CM000663.1:g.159683624T>A	GRCh37
NC_000001.9:g.157950248T>A	NCBI36
NG_013007.1:g.5756A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.366A>T MANE Select	ENSP00000255030.5:p.Ser122=
ENST00000368110.1:c.193+173A>T	ENSP00000357091.1:n.193+173A>T
ENST00000368111.5:c.193+173A>T	ENSP00000357092.1:n.193+173A>T
ENST00000368112.5:c.197+169A>T	ENSP00000357093.1:n.197+169A>T
ENST00000437342.1:c.-169A>T	ENSP00000402788.1:n.-169A>T
ENST00000489317.1:n.74+173A>T
NM_000567.2:c.366A>T	NP_000558.2:p.Ser122=
XM_011509207.1:c.366A>T	XP_011507509.1:p.Ser122=
NM_001329057.1:c.366A>T	NP_001315986.1:p.Ser122=
NM_001329058.1:c.197+169A>T	NP_001315987.1:n.197+169A>T
NM_000567.3:c.366A>T MANE Select	NP_000558.2:p.Ser122=
NM_001329057.2:c.366A>T	NP_001315986.1:p.Ser122=
NM_001329058.2:c.197+169A>T	NP_001315987.1:n.197+169A>T
NM_001382703.1:c.193+173A>T	NP_001369632.1:n.193+173A>T