Canonical Allele Identifier: CA1619240534

Gene: PRRC2A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635055_31635056delinsTG , CM000668.2:g.31635055_31635056delinsTG	GRCh38
NC_000006.11:g.31602832_31602833delinsTG , CM000668.1:g.31602832_31602833delinsTG	GRCh37
NC_000006.10:g.31710811_31710812delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5161-77_5161-76delinsTG MANE Select	ENSP00000365201.2:n.5161-77_5161-76delinsTG
ENST00000376007.8:c.5161-77_5161-76delinsTG	ENSP00000365175.4:n.5161-77_5161-76delinsTG
ENST00000376033.2:c.5161-77_5161-76delinsTG	ENSP00000365201.2:n.5161-77_5161-76delinsTG
ENST00000484787.1:n.572-77_572-76delinsTG
NM_004638.3:c.5161-77_5161-76delinsTG	NP_004629.3:n.5161-77_5161-76delinsTG
NM_080686.2:c.5161-77_5161-76delinsTG	NP_542417.2:n.5161-77_5161-76delinsTG
XM_011514890.1:c.5161-77_5161-76delinsTG	XP_011513192.1:n.5161-77_5161-76delinsTG
XM_017011274.1:c.5161-77_5161-76delinsTG	XP_016866763.1:n.5161-77_5161-76delinsTG
NM_004638.4:c.5161-77_5161-76delinsTG MANE Select	NP_004629.3:n.5161-77_5161-76delinsTG
NM_080686.3:c.5161-77_5161-76delinsTG	NP_542417.2:n.5161-77_5161-76delinsTG