Canonical Allele Identifier: CA1619235332

Gene: PRRC2A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31622828T= , CM000668.2:g.31622828T=	GRCh38
NC_000006.11:g.31590605T= , CM000668.1:g.31590605T=	GRCh37
NC_000006.10:g.31698584T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706625.1:c.55T=	ENSP00000516471.1:p.Trp19=
ENST00000376033.3:c.39T= MANE Select	ENSP00000365201.2:p.Asp13=
ENST00000376007.8:c.39T=	ENSP00000365175.4:p.Asp13=
ENST00000376033.2:c.39T=	ENSP00000365201.2:p.Asp13=
ENST00000469577.5:n.136-1433T=
NM_004638.3:c.39T=	NP_004629.3:p.Asp13=
NM_080686.2:c.39T=	NP_542417.2:p.Asp13=
XM_011514890.1:c.39T=	XP_011513192.1:p.Asp13=
XM_017011274.1:c.39T=	XP_016866763.1:p.Asp13=
NM_004638.4:c.39T= MANE Select	NP_004629.3:p.Asp13=
NM_080686.3:c.39T=	NP_542417.2:p.Asp13=