Canonical Allele Identifier: CA1619235432
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622905A= , CM000668.2:g.31622905A= GRCh38
NC_000006.11:g.31590682A= , CM000668.1:g.31590682A= GRCh37
NC_000006.10:g.31698661A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.112+4A= MANE Select ENSP00000365201.2:n.112+4A=
ENST00000376007.8:c.112+4A= ENSP00000365175.4:n.112+4A=
ENST00000376033.2:c.112+4A= ENSP00000365201.2:n.112+4A=
ENST00000469577.5:n.136-1356A=
NM_004638.3:c.112+4A= NP_004629.3:n.112+4A=
NM_080686.2:c.112+4A= NP_542417.2:n.112+4A=
XM_011514890.1:c.112+4A= XP_011513192.1:n.112+4A=
XM_017011274.1:c.112+4A= XP_016866763.1:n.112+4A=
NM_004638.4:c.112+4A= MANE Select NP_004629.3:n.112+4A=
NM_080686.3:c.112+4A= NP_542417.2:n.112+4A=