Canonical Allele Identifier: CA1986829058

Gene: PRCP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.82853252T= , CM000673.2:g.82853252T=	GRCh38
NC_000011.9:g.82564294T= , CM000673.1:g.82564294T=	GRCh37
NC_000011.8:g.82241942T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005040.4:c.336A= MANE Select	NP_005031.1:p.Glu112=
ENST00000313010.8:c.336A= MANE Select	ENSP00000317362.3:p.Glu112=
NM_001319214.1:c.21A=	NP_001306143.1:p.Glu7=
NM_001319214.2:c.21A=	NP_001306143.1:p.Glu7=
NM_005040.2:c.336A=	NP_005031.1:p.Glu112=
NM_005040.3:c.336A=	NP_005031.1:p.Glu112=
NM_199418.2:c.399A=	NP_955450.2:p.Glu133=
NM_199418.3:c.399A=	NP_955450.2:p.Glu133=
NM_199418.4:c.399A=	NP_955450.2:p.Glu133=
ENST00000313010.7:c.336A=	ENSP00000317362.3:p.Glu112=
ENST00000393399.6:c.399A=	ENSP00000377055.2:p.Glu133=
ENST00000524642.6:n.364A=
ENST00000527444.5:c.21A=	ENSP00000436141.1:p.Glu7=
ENST00000527444.6:n.364A=
ENST00000528082.5:c.21A=	ENSP00000435071.1:p.Glu7=
ENST00000528082.6:c.-10A=	ENSP00000435071.2:n.-10A=
ENST00000529671.5:c.213A=	ENSP00000434771.1:p.Glu71=
ENST00000531128.5:c.21A=	ENSP00000431435.1:p.Glu7=
ENST00000531283.2:n.364A=
ENST00000531801.5:c.21A=	ENSP00000432004.1:p.Glu7=
ENST00000531801.6:c.21A=	ENSP00000432004.2:p.Glu7=
ENST00000532809.1:c.174A=	ENSP00000437169.1:p.Glu58=
ENST00000532809.2:c.174A=	ENSP00000437169.2:p.Glu58=
ENST00000533126.1:c.21A=	ENSP00000431496.1:p.Glu7=
ENST00000534264.1:c.21A=	ENSP00000436095.1:p.Glu7=
ENST00000534264.2:c.21A=	ENSP00000436095.2:p.Glu7=
ENST00000534396.5:c.21A=	ENSP00000432506.1:p.Glu7=
ENST00000534631.5:c.21A=	ENSP00000431559.1:p.Glu7=
ENST00000679387.1:c.21A=	ENSP00000506058.1:p.Glu7=
ENST00000679623.1:c.21A=	ENSP00000506508.1:p.Glu7=
ENST00000680437.1:c.309+6725A=	ENSP00000505089.1:n.309+6725A=
ENST00000680524.1:c.-183-13827A=	ENSP00000506464.1:n.-183-13827A=
ENST00000680566.1:c.21A=	ENSP00000505064.1:p.Glu7=
ENST00000681155.1:n.393A=
ENST00000681322.1:c.336A=	ENSP00000506444.1:p.Glu112=
ENST00000681637.1:c.21A=	ENSP00000506101.1:p.Glu7=
ENST00000681781.1:n.189A=
ENST00000681826.1:n.428A=
XM_005274093.1:c.21A=	XP_005274150.1:p.Glu7=