Canonical Allele Identifier: CA1619235447
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622916A= , CM000668.2:g.31622916A= GRCh38
NC_000006.11:g.31590693A= , CM000668.1:g.31590693A= GRCh37
NC_000006.10:g.31698672A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.112+15A= MANE Select ENSP00000365201.2:n.112+15A=
ENST00000376007.8:c.112+15A= ENSP00000365175.4:n.112+15A=
ENST00000376033.2:c.112+15A= ENSP00000365201.2:n.112+15A=
ENST00000469577.5:n.136-1345A=
NM_004638.3:c.112+15A= NP_004629.3:n.112+15A=
NM_080686.2:c.112+15A= NP_542417.2:n.112+15A=
XM_011514890.1:c.112+15A= XP_011513192.1:n.112+15A=
XM_017011274.1:c.112+15A= XP_016866763.1:n.112+15A=
NM_004638.4:c.112+15A= MANE Select NP_004629.3:n.112+15A=
NM_080686.3:c.112+15A= NP_542417.2:n.112+15A=