Canonical Allele Identifier: CA1619240649

Gene: PRRC2A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635291T= , CM000668.2:g.31635291T=	GRCh38
NC_000006.11:g.31603068T= , CM000668.1:g.31603068T=	GRCh37
NC_000006.10:g.31711047T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5301+19T= MANE Select	ENSP00000365201.2:n.5301+19T=
ENST00000376007.8:c.5301+19T=	ENSP00000365175.4:n.5301+19T=
ENST00000376033.2:c.5301+19T=	ENSP00000365201.2:n.5301+19T=
ENST00000469501.1:n.31+19T=
ENST00000484787.1:n.731T=
NM_004638.3:c.5301+19T=	NP_004629.3:n.5301+19T=
NM_080686.2:c.5301+19T=	NP_542417.2:n.5301+19T=
XM_011514890.1:c.5301+19T=	XP_011513192.1:n.5301+19T=
XM_017011274.1:c.5301+19T=	XP_016866763.1:n.5301+19T=
NM_004638.4:c.5301+19T= MANE Select	NP_004629.3:n.5301+19T=
NM_080686.3:c.5301+19T=	NP_542417.2:n.5301+19T=