Canonical Allele Identifier: CA1619235345
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622846G= , CM000668.2:g.31622846G= GRCh38
NC_000006.11:g.31590623G= , CM000668.1:g.31590623G= GRCh37
NC_000006.10:g.31698602G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000706625.1:c.73G= ENSP00000516471.1:p.Ala25=
ENST00000376033.3:c.57G= MANE Select ENSP00000365201.2:p.Ser19=
ENST00000376007.8:c.57G= ENSP00000365175.4:p.Ser19=
ENST00000376033.2:c.57G= ENSP00000365201.2:p.Ser19=
ENST00000469577.5:n.136-1415G=
NM_004638.3:c.57G= NP_004629.3:p.Ser19=
NM_080686.2:c.57G= NP_542417.2:p.Ser19=
XM_011514890.1:c.57G= XP_011513192.1:p.Ser19=
XM_017011274.1:c.57G= XP_016866763.1:p.Ser19=
NM_004638.4:c.57G= MANE Select NP_004629.3:p.Ser19=
NM_080686.3:c.57G= NP_542417.2:p.Ser19=