Canonical Allele Identifier: CA1202015648

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713783_159713785delinsCAG , CM000663.2:g.159713783_159713785delinsCAG	GRCh38
NC_000001.10:g.159683573_159683575delinsCAG , CM000663.1:g.159683573_159683575delinsCAG	GRCh37
NC_000001.9:g.157950197_157950199delinsCAG	NCBI36
NG_013007.1:g.5805_5807delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.415_417delinsCTG MANE Select	ENSP00000255030.5:p.Leu139=
ENST00000368110.1:c.194-145_194-143delinsCTG	ENSP00000357091.1:n.194-145_194-143delinsCTG
ENST00000368111.5:c.194-145_194-143delinsCTG	ENSP00000357092.1:n.194-145_194-143delinsCTG
ENST00000368112.5:c.198-182_198-180delinsCTG	ENSP00000357093.1:n.198-182_198-180delinsCTG
ENST00000437342.1:c.-120_-118delinsCTG	ENSP00000402788.1:n.-120_-118delinsCTG
ENST00000489317.1:n.74+222_74+224delinsCTG
NM_000567.2:c.415_417delinsCTG	NP_000558.2:p.Leu139=
XM_011509207.1:c.415_417delinsCTG	XP_011507509.1:p.Leu139=
NM_001329057.1:c.415_417delinsCTG	NP_001315986.1:p.Leu139=
NM_001329058.1:c.198-182_198-180delinsCTG	NP_001315987.1:n.198-182_198-180delinsCTG
NM_000567.3:c.415_417delinsCTG MANE Select	NP_000558.2:p.Leu139=
NM_001329057.2:c.415_417delinsCTG	NP_001315986.1:p.Leu139=
NM_001329058.2:c.198-182_198-180delinsCTG	NP_001315987.1:n.198-182_198-180delinsCTG
NM_001382703.1:c.194-145_194-143delinsCTG	NP_001369632.1:n.194-145_194-143delinsCTG