Canonical Allele Identifier: CA2677997067
Gene: PRRC2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622763_31622764del , CM000668.2:g.31622763_31622764del GRCh38
NC_000006.11:g.31590540_31590541del , CM000668.1:g.31590540_31590541del GRCh37
NC_000006.10:g.31698519_31698520del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-27_-26del MANE Select ENSP00000365201.2:n.-27_-26del
ENST00000376007.8:c.-27_-26del ENSP00000365175.4:n.-27_-26del
ENST00000376033.2:c.-27_-26del ENSP00000365201.2:n.-27_-26del
ENST00000469577.5:n.136-1498_136-1497del
NM_004638.3:c.-27_-26del NP_004629.3:n.-27_-26del
NM_080686.2:c.-27_-26del NP_542417.2:n.-27_-26del
XM_011514890.1:c.-27_-26del XP_011513192.1:n.-27_-26del
NM_004638.4:c.-27_-26del MANE Select NP_004629.3:n.-27_-26del
NM_080686.3:c.-27_-26del NP_542417.2:n.-27_-26del