Canonical Allele Identifier: CA1619235425
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622903_31622905delinsTGA , CM000668.2:g.31622903_31622905delinsTGA GRCh38
NC_000006.11:g.31590680_31590682delinsTGA , CM000668.1:g.31590680_31590682delinsTGA GRCh37
NC_000006.10:g.31698659_31698661delinsTGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.112+2_112+4delinsTGA MANE Select ENSP00000365201.2:n.112+2_112+4delinsTGA
ENST00000376007.8:c.112+2_112+4delinsTGA ENSP00000365175.4:n.112+2_112+4delinsTGA
ENST00000376033.2:c.112+2_112+4delinsTGA ENSP00000365201.2:n.112+2_112+4delinsTGA
ENST00000469577.5:n.136-1358_136-1356delinsTGA
NM_004638.3:c.112+2_112+4delinsTGA NP_004629.3:n.112+2_112+4delinsTGA
NM_080686.2:c.112+2_112+4delinsTGA NP_542417.2:n.112+2_112+4delinsTGA
XM_011514890.1:c.112+2_112+4delinsTGA XP_011513192.1:n.112+2_112+4delinsTGA
XM_017011274.1:c.112+2_112+4delinsTGA XP_016866763.1:n.112+2_112+4delinsTGA
NM_004638.4:c.112+2_112+4delinsTGA MANE Select NP_004629.3:n.112+2_112+4delinsTGA
NM_080686.3:c.112+2_112+4delinsTGA NP_542417.2:n.112+2_112+4delinsTGA