Canonical Allele Identifier: CA2578565763
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622786C>A , CM000668.2:g.31622786C>A GRCh38
NC_000006.11:g.31590563C>A , CM000668.1:g.31590563C>A GRCh37
NC_000006.10:g.31698542C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000706625.1:c.13C>A ENSP00000516471.1:p.Arg5Ser
ENST00000376033.3:c.-4C>A MANE Select ENSP00000365201.2:n.-4C>A
ENST00000376007.8:c.-4C>A ENSP00000365175.4:n.-4C>A
ENST00000376033.2:c.-4C>A ENSP00000365201.2:n.-4C>A
ENST00000469577.5:n.136-1475C>A
NM_004638.3:c.-4C>A NP_004629.3:n.-4C>A
NM_080686.2:c.-4C>A NP_542417.2:n.-4C>A
XM_011514890.1:c.-4C>A XP_011513192.1:n.-4C>A
NM_004638.4:c.-4C>A MANE Select NP_004629.3:n.-4C>A
NM_080686.3:c.-4C>A NP_542417.2:n.-4C>A