Canonical Allele Identifier: CA1619235206
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622731T= , CM000668.2:g.31622731T= GRCh38
NC_000006.11:g.31590508T= , CM000668.1:g.31590508T= GRCh37
NC_000006.10:g.31698487T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-59T= MANE Select ENSP00000365201.2:n.-59T=
ENST00000376007.8:c.-59T= ENSP00000365175.4:n.-59T=
ENST00000376033.2:c.-59T= ENSP00000365201.2:n.-59T=
ENST00000469577.5:n.136-1530T=
NM_004638.3:c.-59T= NP_004629.3:n.-59T=
NM_080686.2:c.-59T= NP_542417.2:n.-59T=
XM_011514890.1:c.-59T= XP_011513192.1:n.-59T=
NM_004638.4:c.-59T= MANE Select NP_004629.3:n.-59T=
NM_080686.3:c.-59T= NP_542417.2:n.-59T=