Canonical Allele Identifier: CA2648593762

Gene: CRP

Linked Data

• gnomAD v4: 1-159713711-GTTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713712_159713714del , CM000663.2:g.159713712_159713714del	GRCh38
NC_000001.10:g.159683502_159683504del , CM000663.1:g.159683502_159683504del	GRCh37
NC_000001.9:g.157950126_157950128del	NCBI36
NG_013007.1:g.5876_5878del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.486_488del MANE Select	ENSP00000255030.5:p.Asn163del
ENST00000368110.1:c.194-74_194-72del	ENSP00000357091.1:n.194-74_194-72del
ENST00000368111.5:c.194-74_194-72del	ENSP00000357092.1:n.194-74_194-72del
ENST00000368112.5:c.198-111_198-109del	ENSP00000357093.1:n.198-111_198-109del
ENST00000437342.1:c.-49_-47del	ENSP00000402788.1:n.-49_-47del
ENST00000473196.1:n.54_56del
ENST00000489317.1:n.74+293_74+295del
NM_000567.2:c.486_488del	NP_000558.2:p.Asn163del
XM_011509207.1:c.486_488del	XP_011507509.1:p.Asn163del
NM_001329057.1:c.486_488del	NP_001315986.1:p.Asn163del
NM_001329058.1:c.198-111_198-109del	NP_001315987.1:n.198-111_198-109del
NM_000567.3:c.486_488del MANE Select	NP_000558.2:p.Asn163del
NM_001329057.2:c.486_488del	NP_001315986.1:p.Asn163del
NM_001329058.2:c.198-111_198-109del	NP_001315987.1:n.198-111_198-109del
NM_001382703.1:c.194-74_194-72del	NP_001369632.1:n.194-74_194-72del