Canonical Allele Identifier: CA1202015829

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713894_159713897delinsGAAT , CM000663.2:g.159713894_159713897delinsGAAT	GRCh38
NC_000001.10:g.159683684_159683687delinsGAAT , CM000663.1:g.159683684_159683687delinsGAAT	GRCh37
NC_000001.9:g.157950308_157950311delinsGAAT	NCBI36
NG_013007.1:g.5693_5696delinsATTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.303_306delinsATTC MANE Select	ENSP00000255030.5:p.Leu101=
ENST00000368110.1:c.193+110_193+113delinsATTC	ENSP00000357091.1:n.193+110_193+113delinsATTC
ENST00000368111.5:c.193+110_193+113delinsATTC	ENSP00000357092.1:n.193+110_193+113delinsATTC
ENST00000368112.5:c.197+106_197+109delinsATTC	ENSP00000357093.1:n.197+106_197+109delinsATTC
ENST00000437342.1:c.-232_-229delinsATTC	ENSP00000402788.1:n.-232_-229delinsATTC
ENST00000489317.1:n.74+110_74+113delinsATTC
NM_000567.2:c.303_306delinsATTC	NP_000558.2:p.Leu101=
XM_011509207.1:c.303_306delinsATTC	XP_011507509.1:p.Leu101=
NM_001329057.1:c.303_306delinsATTC	NP_001315986.1:p.Leu101=
NM_001329058.1:c.197+106_197+109delinsATTC	NP_001315987.1:n.197+106_197+109delinsATTC
NM_000567.3:c.303_306delinsATTC MANE Select	NP_000558.2:p.Leu101=
NM_001329057.2:c.303_306delinsATTC	NP_001315986.1:p.Leu101=
NM_001329058.2:c.197+106_197+109delinsATTC	NP_001315987.1:n.197+106_197+109delinsATTC
NM_001382703.1:c.193+110_193+113delinsATTC	NP_001369632.1:n.193+110_193+113delinsATTC