Canonical Allele Identifier: CA2501860129

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159714562_159714563insC , CM000663.2:g.159714562_159714563insC	GRCh38
NC_000001.10:g.159684352_159684353insC , CM000663.1:g.159684352_159684353insC	GRCh37
NC_000001.9:g.157950976_157950977insC	NCBI36
NG_013007.1:g.5027_5028insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.-78_-77insG MANE Select	ENSP00000255030.5:n.-78_-77insG
ENST00000368110.1:c.-78_-77insG	ENSP00000357091.1:n.-78_-77insG
ENST00000368111.5:c.-78_-77insG	ENSP00000357092.1:n.-78_-77insG
ENST00000368112.5:c.-78_-77insG	ENSP00000357093.1:n.-78_-77insG
ENST00000437342.1:c.-372_-371insG	ENSP00000402788.1:n.-372_-371insG
NM_000567.2:c.-78_-77insG	NP_000558.2:n.-78_-77insG
XM_011509207.1:c.-78_-77insG	XP_011507509.1:n.-78_-77insG
NM_001329057.1:c.-78_-77insG	NP_001315986.1:n.-78_-77insG
NM_001329058.1:c.-78_-77insG	NP_001315987.1:n.-78_-77insG
NM_000567.3:c.-78_-77insG MANE Select	NP_000558.2:n.-78_-77insG
NM_001329057.2:c.-78_-77insG	NP_001315986.1:n.-78_-77insG
NM_001329058.2:c.-78_-77insG	NP_001315987.1:n.-78_-77insG
NM_001382703.1:c.-78_-77insG	NP_001369632.1:n.-78_-77insG