Canonical Allele Identifier: CA1619240508
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31635016A= , CM000668.2:g.31635016A= GRCh38
NC_000006.11:g.31602793A= , CM000668.1:g.31602793A= GRCh37
NC_000006.10:g.31710772A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5160+39A= MANE Select ENSP00000365201.2:n.5160+39A=
ENST00000376007.8:c.5160+39A= ENSP00000365175.4:n.5160+39A=
ENST00000376033.2:c.5160+39A= ENSP00000365201.2:n.5160+39A=
ENST00000484787.1:n.571+39A=
NM_004638.3:c.5160+39A= NP_004629.3:n.5160+39A=
NM_080686.2:c.5160+39A= NP_542417.2:n.5160+39A=
XM_011514890.1:c.5160+39A= XP_011513192.1:n.5160+39A=
XM_017011274.1:c.5160+39A= XP_016866763.1:n.5160+39A=
NM_004638.4:c.5160+39A= MANE Select NP_004629.3:n.5160+39A=
NM_080686.3:c.5160+39A= NP_542417.2:n.5160+39A=