Canonical Allele Identifier: CA2677997035
Gene: PRRC2A HGNC NCBI

Linked Data

gnomAD v4: 6-31622708-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622710del , CM000668.2:g.31622710del GRCh38
NC_000006.11:g.31590487del , CM000668.1:g.31590487del GRCh37
NC_000006.10:g.31698466del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-80del MANE Select ENSP00000365201.2:n.-80del
ENST00000376007.8:c.-63-17del ENSP00000365175.4:n.-63-17del
ENST00000376033.2:c.-80del ENSP00000365201.2:n.-80del
ENST00000469577.5:n.136-1551del
NM_004638.3:c.-80del NP_004629.3:n.-80del
NM_080686.2:c.-63-17del NP_542417.2:n.-63-17del
XM_011514890.1:c.-63-17del XP_011513192.1:n.-63-17del
NM_004638.4:c.-80del MANE Select NP_004629.3:n.-80del
NM_080686.3:c.-63-17del NP_542417.2:n.-63-17del
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