Canonical Allele Identifier: CA1619241681
Community Standard Title: NM_004638.4(PRRC2A):c.6334-24G=
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31637422G= , CM000668.2:g.31637422G= GRCh38
NC_000006.11:g.31605199G= , CM000668.1:g.31605199G= GRCh37
NC_000006.10:g.31713178G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_004638.4:c.6334-24G= MANE Select NP_004629.3:n.6334-24G=
ENST00000376033.3:c.6334-24G= MANE Select ENSP00000365201.2:n.6334-24G=
NM_004638.3:c.6334-24G= NP_004629.3:n.6334-24G=
NM_080686.2:c.6334-24G= NP_542417.2:n.6334-24G=
NM_080686.3:c.6334-24G= NP_542417.2:n.6334-24G=
ENST00000376007.8:c.6334-24G= ENSP00000365175.4:n.6334-24G=
ENST00000376033.2:c.6334-24G= ENSP00000365201.2:n.6334-24G=
ENST00000462617.1:n.666G=
ENST00000482441.1:n.394-24G=
ENST00000492691.5:n.769G=
XM_011514890.1:c.6121-24G= XP_011513192.1:n.6121-24G=
XM_017011274.1:c.6121-24G= XP_016866763.1:n.6121-24G=