Canonical Allele Identifier: CA1619235511
Gene: PRRC2A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622980G= , CM000668.2:g.31622980G= GRCh38
NC_000006.11:g.31590757G= , CM000668.1:g.31590757G= GRCh37
NC_000006.10:g.31698736G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.112+79G= MANE Select ENSP00000365201.2:n.112+79G=
ENST00000376007.8:c.112+79G= ENSP00000365175.4:n.112+79G=
ENST00000376033.2:c.112+79G= ENSP00000365201.2:n.112+79G=
ENST00000469577.5:n.136-1281G=
NM_004638.3:c.112+79G= NP_004629.3:n.112+79G=
NM_080686.2:c.112+79G= NP_542417.2:n.112+79G=
XM_011514890.1:c.112+79G= XP_011513192.1:n.112+79G=
XM_017011274.1:c.112+79G= XP_016866763.1:n.112+79G=
NM_004638.4:c.112+79G= MANE Select NP_004629.3:n.112+79G=
NM_080686.3:c.112+79G= NP_542417.2:n.112+79G=
Search 100 bp 5'
Search 100 bp 3'