Canonical Allele Identifier: CA1619235402
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622891G= , CM000668.2:g.31622891G= GRCh38
NC_000006.11:g.31590668G= , CM000668.1:g.31590668G= GRCh37
NC_000006.10:g.31698647G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.102G= MANE Select ENSP00000365201.2:p.Gln34=
ENST00000376007.8:c.102G= ENSP00000365175.4:p.Gln34=
ENST00000376033.2:c.102G= ENSP00000365201.2:p.Gln34=
ENST00000469577.5:n.136-1370G=
NM_004638.3:c.102G= NP_004629.3:p.Gln34=
NM_080686.2:c.102G= NP_542417.2:p.Gln34=
XM_011514890.1:c.102G= XP_011513192.1:p.Gln34=
XM_017011274.1:c.102G= XP_016866763.1:p.Gln34=
NM_004638.4:c.102G= MANE Select NP_004629.3:p.Gln34=
NM_080686.3:c.102G= NP_542417.2:p.Gln34=