Canonical Allele Identifier: CA1619240636
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31635272G= , CM000668.2:g.31635272G= GRCh38
NC_000006.11:g.31603049G= , CM000668.1:g.31603049G= GRCh37
NC_000006.10:g.31711028G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5301G= MANE Select ENSP00000365201.2:p.Lys1767=
ENST00000376007.8:c.5301G= ENSP00000365175.4:p.Lys1767=
ENST00000376033.2:c.5301G= ENSP00000365201.2:p.Lys1767=
ENST00000469501.1:n.31G=
ENST00000484787.1:n.712G=
NM_004638.3:c.5301G= NP_004629.3:p.Lys1767=
NM_080686.2:c.5301G= NP_542417.2:p.Lys1767=
XM_011514890.1:c.5301G= XP_011513192.1:p.Lys1767=
XM_017011274.1:c.5301G= XP_016866763.1:p.Lys1767=
NM_004638.4:c.5301G= MANE Select NP_004629.3:p.Lys1767=
NM_080686.3:c.5301G= NP_542417.2:p.Lys1767=