Canonical Allele Identifier: CA1619235499
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622959C= , CM000668.2:g.31622959C= GRCh38
NC_000006.11:g.31590736C= , CM000668.1:g.31590736C= GRCh37
NC_000006.10:g.31698715C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.112+58C= MANE Select ENSP00000365201.2:n.112+58C=
ENST00000376007.8:c.112+58C= ENSP00000365175.4:n.112+58C=
ENST00000376033.2:c.112+58C= ENSP00000365201.2:n.112+58C=
ENST00000469577.5:n.136-1302C=
NM_004638.3:c.112+58C= NP_004629.3:n.112+58C=
NM_080686.2:c.112+58C= NP_542417.2:n.112+58C=
XM_011514890.1:c.112+58C= XP_011513192.1:n.112+58C=
XM_017011274.1:c.112+58C= XP_016866763.1:n.112+58C=
NM_004638.4:c.112+58C= MANE Select NP_004629.3:n.112+58C=
NM_080686.3:c.112+58C= NP_542417.2:n.112+58C=