Canonical Allele Identifier: CA1619235542

Gene: PRRC2A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31623026_31623027delinsAC , CM000668.2:g.31623026_31623027delinsAC	GRCh38
NC_000006.11:g.31590803_31590804delinsAC , CM000668.1:g.31590803_31590804delinsAC	GRCh37
NC_000006.10:g.31698782_31698783delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376033.3:c.112+125_112+126delinsAC MANE Select	ENSP00000365201.2:n.112+125_112+126delinsAC
ENST00000376007.8:c.112+125_112+126delinsAC	ENSP00000365175.4:n.112+125_112+126delinsAC
ENST00000376033.2:c.112+125_112+126delinsAC	ENSP00000365201.2:n.112+125_112+126delinsAC
ENST00000469577.5:n.136-1235_136-1234delinsAC
NM_004638.3:c.112+125_112+126delinsAC	NP_004629.3:n.112+125_112+126delinsAC
NM_080686.2:c.112+125_112+126delinsAC	NP_542417.2:n.112+125_112+126delinsAC
XM_011514890.1:c.112+125_112+126delinsAC	XP_011513192.1:n.112+125_112+126delinsAC
XM_017011274.1:c.112+125_112+126delinsAC	XP_016866763.1:n.112+125_112+126delinsAC
NM_004638.4:c.112+125_112+126delinsAC MANE Select	NP_004629.3:n.112+125_112+126delinsAC
NM_080686.3:c.112+125_112+126delinsAC	NP_542417.2:n.112+125_112+126delinsAC