Canonical Allele Identifier: CA1619235224
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs1775434966

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622745_31622752del , CM000668.2:g.31622745_31622752del GRCh38
NC_000006.11:g.31590522_31590529del , CM000668.1:g.31590522_31590529del GRCh37
NC_000006.10:g.31698501_31698508del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-45_-38del MANE Select ENSP00000365201.2:n.-45_-38del
ENST00000376007.8:c.-45_-38del ENSP00000365175.4:n.-45_-38del
ENST00000376033.2:c.-45_-38del ENSP00000365201.2:n.-45_-38del
ENST00000469577.5:n.136-1516_136-1509del
NM_004638.3:c.-45_-38del NP_004629.3:n.-45_-38del
NM_080686.2:c.-45_-38del NP_542417.2:n.-45_-38del
XM_011514890.1:c.-45_-38del XP_011513192.1:n.-45_-38del
NM_004638.4:c.-45_-38del MANE Select NP_004629.3:n.-45_-38del
NM_080686.3:c.-45_-38del NP_542417.2:n.-45_-38del