Canonical Allele Identifier: CA2677997026
Gene: PRRC2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622698_31622699del , CM000668.2:g.31622698_31622699del GRCh38
NC_000006.11:g.31590475_31590476del , CM000668.1:g.31590475_31590476del GRCh37
NC_000006.10:g.31698454_31698455del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-92_-91del MANE Select ENSP00000365201.2:n.-92_-91del
ENST00000376007.8:c.-63-29_-63-28del ENSP00000365175.4:n.-63-29_-63-28del
ENST00000376033.2:c.-92_-91del ENSP00000365201.2:n.-92_-91del
ENST00000469577.5:n.136-1563_136-1562del
NM_004638.3:c.-92_-91del NP_004629.3:n.-92_-91del
NM_080686.2:c.-63-29_-63-28del NP_542417.2:n.-63-29_-63-28del
XM_011514890.1:c.-63-29_-63-28del XP_011513192.1:n.-63-29_-63-28del
NM_004638.4:c.-92_-91del MANE Select NP_004629.3:n.-92_-91del
NM_080686.3:c.-63-29_-63-28del NP_542417.2:n.-63-29_-63-28del