Canonical Allele Identifier: CA2574073722

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713760_159713774dup , CM000663.2:g.159713760_159713774dup	GRCh38
NC_000001.10:g.159683550_159683564dup , CM000663.1:g.159683550_159683564dup	GRCh37
NC_000001.9:g.157950174_157950188dup	NCBI36
NG_013007.1:g.5817_5831dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.427_441dup MANE Select	ENSP00000255030.5:p.Ala147_Glu148insTyrThrValGlyAla
ENST00000368110.1:c.194-133_194-119dup	ENSP00000357091.1:n.194-133_194-119dup
ENST00000368111.5:c.194-133_194-119dup	ENSP00000357092.1:n.194-133_194-119dup
ENST00000368112.5:c.198-170_198-156dup	ENSP00000357093.1:n.198-170_198-156dup
ENST00000437342.1:c.-108_-94dup	ENSP00000402788.1:n.-108_-94dup
ENST00000489317.1:n.74+234_74+248dup
NM_000567.2:c.427_441dup	NP_000558.2:p.Ala147_Glu148insTyrThrValGlyAla
XM_011509207.1:c.427_441dup	XP_011507509.1:p.Ala147_Glu148insTyrThrValGlyAla
NM_001329057.1:c.427_441dup	NP_001315986.1:p.Ala147_Glu148insTyrThrValGlyAla
NM_001329058.1:c.198-170_198-156dup	NP_001315987.1:n.198-170_198-156dup
NM_000567.3:c.427_441dup MANE Select	NP_000558.2:p.Ala147_Glu148insTyrThrValGlyAla
NM_001329057.2:c.427_441dup	NP_001315986.1:p.Ala147_Glu148insTyrThrValGlyAla
NM_001329058.2:c.198-170_198-156dup	NP_001315987.1:n.198-170_198-156dup
NM_001382703.1:c.194-133_194-119dup	NP_001369632.1:n.194-133_194-119dup