Canonical Allele Identifier: CA2648593765

Gene: CRP

Linked Data

• gnomAD v4: 1-159713720-G-GCC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713720_159713721insCC , CM000663.2:g.159713720_159713721insCC	GRCh38
NC_000001.10:g.159683510_159683511insCC , CM000663.1:g.159683510_159683511insCC	GRCh37
NC_000001.9:g.157950134_157950135insCC	NCBI36
NG_013007.1:g.5869_5870insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.479_480insGG MANE Select	ENSP00000255030.5:p.Phe160LeufsTer19
ENST00000368110.1:c.194-81_194-80insGG	ENSP00000357091.1:n.194-81_194-80insGG
ENST00000368111.5:c.194-81_194-80insGG	ENSP00000357092.1:n.194-81_194-80insGG
ENST00000368112.5:c.198-118_198-117insGG	ENSP00000357093.1:n.198-118_198-117insGG
ENST00000437342.1:c.-56_-55insGG	ENSP00000402788.1:n.-56_-55insGG
ENST00000473196.1:n.47_48insGG
ENST00000489317.1:n.74+286_74+287insGG
NM_000567.2:c.479_480insGG	NP_000558.2:p.Phe160LeufsTer19
XM_011509207.1:c.479_480insGG	XP_011507509.1:p.Phe160LeufsTer19
NM_001329057.1:c.479_480insGG	NP_001315986.1:p.Phe160LeufsTer19
NM_001329058.1:c.198-118_198-117insGG	NP_001315987.1:n.198-118_198-117insGG
NM_000567.3:c.479_480insGG MANE Select	NP_000558.2:p.Phe160LeufsTer19
NM_001329057.2:c.479_480insGG	NP_001315986.1:p.Phe160LeufsTer19
NM_001329058.2:c.198-118_198-117insGG	NP_001315987.1:n.198-118_198-117insGG
NM_001382703.1:c.194-81_194-80insGG	NP_001369632.1:n.194-81_194-80insGG