Canonical Allele Identifier: CA1619235349
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622847C= , CM000668.2:g.31622847C= GRCh38
NC_000006.11:g.31590624C= , CM000668.1:g.31590624C= GRCh37
NC_000006.10:g.31698603C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000706625.1:c.74C= ENSP00000516471.1:p.Ala25=
ENST00000376033.3:c.58C= MANE Select ENSP00000365201.2:p.Leu20=
ENST00000376007.8:c.58C= ENSP00000365175.4:p.Leu20=
ENST00000376033.2:c.58C= ENSP00000365201.2:p.Leu20=
ENST00000469577.5:n.136-1414C=
NM_004638.3:c.58C= NP_004629.3:p.Leu20=
NM_080686.2:c.58C= NP_542417.2:p.Leu20=
XM_011514890.1:c.58C= XP_011513192.1:p.Leu20=
XM_017011274.1:c.58C= XP_016866763.1:p.Leu20=
NM_004638.4:c.58C= MANE Select NP_004629.3:p.Leu20=
NM_080686.3:c.58C= NP_542417.2:p.Leu20=