Canonical Allele Identifier: CA1619240623
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31635242T= , CM000668.2:g.31635242T= GRCh38
NC_000006.11:g.31603019T= , CM000668.1:g.31603019T= GRCh37
NC_000006.10:g.31710998T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5271T= MANE Select ENSP00000365201.2:p.Gly1757=
ENST00000376007.8:c.5271T= ENSP00000365175.4:p.Gly1757=
ENST00000376033.2:c.5271T= ENSP00000365201.2:p.Gly1757=
ENST00000469501.1:n.1T=
ENST00000484787.1:n.682T=
NM_004638.3:c.5271T= NP_004629.3:p.Gly1757=
NM_080686.2:c.5271T= NP_542417.2:p.Gly1757=
XM_011514890.1:c.5271T= XP_011513192.1:p.Gly1757=
XM_017011274.1:c.5271T= XP_016866763.1:p.Gly1757=
NM_004638.4:c.5271T= MANE Select NP_004629.3:p.Gly1757=
NM_080686.3:c.5271T= NP_542417.2:p.Gly1757=