Canonical Allele Identifier: CA1619235159
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622706C= , CM000668.2:g.31622706C= GRCh38
NC_000006.11:g.31590483C= , CM000668.1:g.31590483C= GRCh37
NC_000006.10:g.31698462C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-84C= MANE Select ENSP00000365201.2:n.-84C=
ENST00000376007.8:c.-63-21C= ENSP00000365175.4:n.-63-21C=
ENST00000376033.2:c.-84C= ENSP00000365201.2:n.-84C=
ENST00000469577.5:n.136-1555C=
NM_004638.3:c.-84C= NP_004629.3:n.-84C=
NM_080686.2:c.-63-21C= NP_542417.2:n.-63-21C=
XM_011514890.1:c.-63-21C= XP_011513192.1:n.-63-21C=
NM_004638.4:c.-84C= MANE Select NP_004629.3:n.-84C=
NM_080686.3:c.-63-21C= NP_542417.2:n.-63-21C=