Canonical Allele Identifier: CA1619235268
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622781T= , CM000668.2:g.31622781T= GRCh38
NC_000006.11:g.31590558T= , CM000668.1:g.31590558T= GRCh37
NC_000006.10:g.31698537T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000706625.1:c.8T= ENSP00000516471.1:p.Phe3=
ENST00000376033.3:c.-9T= MANE Select ENSP00000365201.2:n.-9T=
ENST00000376007.8:c.-9T= ENSP00000365175.4:n.-9T=
ENST00000376033.2:c.-9T= ENSP00000365201.2:n.-9T=
ENST00000469577.5:n.136-1480T=
NM_004638.3:c.-9T= NP_004629.3:n.-9T=
NM_080686.2:c.-9T= NP_542417.2:n.-9T=
XM_011514890.1:c.-9T= XP_011513192.1:n.-9T=
NM_004638.4:c.-9T= MANE Select NP_004629.3:n.-9T=
NM_080686.3:c.-9T= NP_542417.2:n.-9T=