Canonical Allele Identifier: CA1619235359

Gene: PRRC2A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31622852C= , CM000668.2:g.31622852C=	GRCh38
NC_000006.11:g.31590629C= , CM000668.1:g.31590629C=	GRCh37
NC_000006.10:g.31698608C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706625.1:c.79C=	ENSP00000516471.1:p.Pro27=
ENST00000376033.3:c.63C= MANE Select	ENSP00000365201.2:p.Asn21=
ENST00000376007.8:c.63C=	ENSP00000365175.4:p.Asn21=
ENST00000376033.2:c.63C=	ENSP00000365201.2:p.Asn21=
ENST00000469577.5:n.136-1409C=
NM_004638.3:c.63C=	NP_004629.3:p.Asn21=
NM_080686.2:c.63C=	NP_542417.2:p.Asn21=
XM_011514890.1:c.63C=	XP_011513192.1:p.Asn21=
XM_017011274.1:c.63C=	XP_016866763.1:p.Asn21=
NM_004638.4:c.63C= MANE Select	NP_004629.3:p.Asn21=
NM_080686.3:c.63C=	NP_542417.2:p.Asn21=