Canonical Allele Identifier: CA2520786458
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31623010_31623011del , CM000668.2:g.31623010_31623011del GRCh38
NC_000006.11:g.31590787_31590788del , CM000668.1:g.31590787_31590788del GRCh37
NC_000006.10:g.31698766_31698767del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.112+109_112+110del MANE Select ENSP00000365201.2:n.112+109_112+110del
ENST00000376007.8:c.112+109_112+110del ENSP00000365175.4:n.112+109_112+110del
ENST00000376033.2:c.112+109_112+110del ENSP00000365201.2:n.112+109_112+110del
ENST00000469577.5:n.136-1251_136-1250del
NM_004638.3:c.112+109_112+110del NP_004629.3:n.112+109_112+110del
NM_080686.2:c.112+109_112+110del NP_542417.2:n.112+109_112+110del
XM_011514890.1:c.112+109_112+110del XP_011513192.1:n.112+109_112+110del
XM_017011274.1:c.112+109_112+110del XP_016866763.1:n.112+109_112+110del
NM_004638.4:c.112+109_112+110del MANE Select NP_004629.3:n.112+109_112+110del
NM_080686.3:c.112+109_112+110del NP_542417.2:n.112+109_112+110del