Canonical Allele Identifier: CA2648593779

Gene: CRP

Linked Data

• gnomAD v4: 1-159713874-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713874_159713875insG , CM000663.2:g.159713874_159713875insG	GRCh38
NC_000001.10:g.159683664_159683665insG , CM000663.1:g.159683664_159683665insG	GRCh37
NC_000001.9:g.157950288_157950289insG	NCBI36
NG_013007.1:g.5715_5716insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.325_326insC MANE Select	ENSP00000255030.5:p.Val109AlafsTer?
ENST00000368110.1:c.193+132_193+133insC	ENSP00000357091.1:n.193+132_193+133insC
ENST00000368111.5:c.193+132_193+133insC	ENSP00000357092.1:n.193+132_193+133insC
ENST00000368112.5:c.197+128_197+129insC	ENSP00000357093.1:n.197+128_197+129insC
ENST00000437342.1:c.-210_-209insC	ENSP00000402788.1:n.-210_-209insC
ENST00000489317.1:n.74+132_74+133insC
NM_000567.2:c.325_326insC	NP_000558.2:p.Val109AlafsTer?
XM_011509207.1:c.325_326insC	XP_011507509.1:p.Val109AlafsTer?
NM_001329057.1:c.325_326insC	NP_001315986.1:p.Val109AlafsTer?
NM_001329058.1:c.197+128_197+129insC	NP_001315987.1:n.197+128_197+129insC
NM_000567.3:c.325_326insC MANE Select	NP_000558.2:p.Val109AlafsTer?
NM_001329057.2:c.325_326insC	NP_001315986.1:p.Val109AlafsTer?
NM_001329058.2:c.197+128_197+129insC	NP_001315987.1:n.197+128_197+129insC
NM_001382703.1:c.193+132_193+133insC	NP_001369632.1:n.193+132_193+133insC