Canonical Allele Identifier: CA1619235177
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622718G= , CM000668.2:g.31622718G= GRCh38
NC_000006.11:g.31590495G= , CM000668.1:g.31590495G= GRCh37
NC_000006.10:g.31698474G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-72G= MANE Select ENSP00000365201.2:n.-72G=
ENST00000376007.8:c.-63-9G= ENSP00000365175.4:n.-63-9G=
ENST00000376033.2:c.-72G= ENSP00000365201.2:n.-72G=
ENST00000469577.5:n.136-1543G=
NM_004638.3:c.-72G= NP_004629.3:n.-72G=
NM_080686.2:c.-63-9G= NP_542417.2:n.-63-9G=
XM_011514890.1:c.-63-9G= XP_011513192.1:n.-63-9G=
NM_004638.4:c.-72G= MANE Select NP_004629.3:n.-72G=
NM_080686.3:c.-63-9G= NP_542417.2:n.-63-9G=