Canonical Allele Identifier: CA1087462965
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs1775431540
gnomAD v3: 6-31622719-GC-G
gnomAD v4: 6-31622719-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622722del , CM000668.2:g.31622722del GRCh38
NC_000006.11:g.31590499del , CM000668.1:g.31590499del GRCh37
NC_000006.10:g.31698478del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-68del MANE Select ENSP00000365201.2:n.-68del
ENST00000376007.8:c.-63-5del ENSP00000365175.4:n.-63-5del
ENST00000376033.2:c.-68del ENSP00000365201.2:n.-68del
ENST00000469577.5:n.136-1539del
NM_004638.3:c.-68del NP_004629.3:n.-68del
NM_080686.2:c.-63-5del NP_542417.2:n.-63-5del
XM_011514890.1:c.-63-5del XP_011513192.1:n.-63-5del
NM_004638.4:c.-68del MANE Select NP_004629.3:n.-68del
NM_080686.3:c.-63-5del NP_542417.2:n.-63-5del
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