Canonical Allele Identifier: CA2832538802

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713765dup , CM000663.2:g.159713765dup	GRCh38
NC_000001.10:g.159683555dup , CM000663.1:g.159683555dup	GRCh37
NC_000001.9:g.157950179dup	NCBI36
NG_013007.1:g.5829dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.439dup MANE Select	ENSP00000255030.5:p.Ala147GlyfsTer19
ENST00000368110.1:c.194-121dup	ENSP00000357091.1:n.194-121dup
ENST00000368111.5:c.194-121dup	ENSP00000357092.1:n.194-121dup
ENST00000368112.5:c.198-158dup	ENSP00000357093.1:n.198-158dup
ENST00000437342.1:c.-96dup	ENSP00000402788.1:n.-96dup
ENST00000473196.1:n.7dup
ENST00000489317.1:n.74+246dup
NM_000567.2:c.439dup	NP_000558.2:p.Ala147GlyfsTer19
XM_011509207.1:c.439dup	XP_011507509.1:p.Ala147GlyfsTer19
NM_001329057.1:c.439dup	NP_001315986.1:p.Ala147GlyfsTer19
NM_001329058.1:c.198-158dup	NP_001315987.1:n.198-158dup
NM_000567.3:c.439dup MANE Select	NP_000558.2:p.Ala147GlyfsTer19
NM_001329057.2:c.439dup	NP_001315986.1:p.Ala147GlyfsTer19
NM_001329058.2:c.198-158dup	NP_001315987.1:n.198-158dup
NM_001382703.1:c.194-121dup	NP_001369632.1:n.194-121dup