Canonical Allele Identifier: CA1619240634
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31635269C= , CM000668.2:g.31635269C= GRCh38
NC_000006.11:g.31603046C= , CM000668.1:g.31603046C= GRCh37
NC_000006.10:g.31711025C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5298C= MANE Select ENSP00000365201.2:p.Asp1766=
ENST00000376007.8:c.5298C= ENSP00000365175.4:p.Asp1766=
ENST00000376033.2:c.5298C= ENSP00000365201.2:p.Asp1766=
ENST00000469501.1:n.28C=
ENST00000484787.1:n.709C=
NM_004638.3:c.5298C= NP_004629.3:p.Asp1766=
NM_080686.2:c.5298C= NP_542417.2:p.Asp1766=
XM_011514890.1:c.5298C= XP_011513192.1:p.Asp1766=
XM_017011274.1:c.5298C= XP_016866763.1:p.Asp1766=
NM_004638.4:c.5298C= MANE Select NP_004629.3:p.Asp1766=
NM_080686.3:c.5298C= NP_542417.2:p.Asp1766=