Canonical Allele Identifier: CA1619240454
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31634935T= , CM000668.2:g.31634935T= GRCh38
NC_000006.11:g.31602712T= , CM000668.1:g.31602712T= GRCh37
NC_000006.10:g.31710691T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5118T= MANE Select ENSP00000365201.2:p.Pro1706=
ENST00000376007.8:c.5118T= ENSP00000365175.4:p.Pro1706=
ENST00000376033.2:c.5118T= ENSP00000365201.2:p.Pro1706=
ENST00000484787.1:n.529T=
NM_004638.3:c.5118T= NP_004629.3:p.Pro1706=
NM_080686.2:c.5118T= NP_542417.2:p.Pro1706=
XM_011514890.1:c.5118T= XP_011513192.1:p.Pro1706=
XM_017011274.1:c.5118T= XP_016866763.1:p.Pro1706=
NM_004638.4:c.5118T= MANE Select NP_004629.3:p.Pro1706=
NM_080686.3:c.5118T= NP_542417.2:p.Pro1706=