Canonical Allele Identifier: CA421618603

Gene: CRP

Linked Data

• MyVariant Identifiers: chr1:g.159683603T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713813T>A , CM000663.2:g.159713813T>A	GRCh38
NC_000001.10:g.159683603T>A , CM000663.1:g.159683603T>A	GRCh37
NC_000001.9:g.157950227T>A	NCBI36
NG_013007.1:g.5777A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.387A>T MANE Select	ENSP00000255030.5:p.Val129=
ENST00000368110.1:c.194-173A>T	ENSP00000357091.1:n.194-173A>T
ENST00000368111.5:c.194-173A>T	ENSP00000357092.1:n.194-173A>T
ENST00000368112.5:c.197+190A>T	ENSP00000357093.1:n.197+190A>T
ENST00000437342.1:c.-148A>T	ENSP00000402788.1:n.-148A>T
ENST00000489317.1:n.74+194A>T
NM_000567.2:c.387A>T	NP_000558.2:p.Val129=
XM_011509207.1:c.387A>T	XP_011507509.1:p.Val129=
NM_001329057.1:c.387A>T	NP_001315986.1:p.Val129=
NM_001329058.1:c.197+190A>T	NP_001315987.1:n.197+190A>T
NM_000567.3:c.387A>T MANE Select	NP_000558.2:p.Val129=
NM_001329057.2:c.387A>T	NP_001315986.1:p.Val129=
NM_001329058.2:c.197+190A>T	NP_001315987.1:n.197+190A>T
NM_001382703.1:c.194-173A>T	NP_001369632.1:n.194-173A>T