Canonical Allele Identifier: CA1619235365
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622861T= , CM000668.2:g.31622861T= GRCh38
NC_000006.11:g.31590638T= , CM000668.1:g.31590638T= GRCh37
NC_000006.10:g.31698617T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.72T= MANE Select ENSP00000365201.2:p.Asp24=
ENST00000376007.8:c.72T= ENSP00000365175.4:p.Asp24=
ENST00000376033.2:c.72T= ENSP00000365201.2:p.Asp24=
ENST00000469577.5:n.136-1400T=
NM_004638.3:c.72T= NP_004629.3:p.Asp24=
NM_080686.2:c.72T= NP_542417.2:p.Asp24=
XM_011514890.1:c.72T= XP_011513192.1:p.Asp24=
XM_017011274.1:c.72T= XP_016866763.1:p.Asp24=
NM_004638.4:c.72T= MANE Select NP_004629.3:p.Asp24=
NM_080686.3:c.72T= NP_542417.2:p.Asp24=