Canonical Allele Identifier: CA2677997151
Gene: PRRC2A HGNC NCBI

Linked Data

gnomAD v4: 6-31623047-AG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31623052del , CM000668.2:g.31623052del GRCh38
NC_000006.11:g.31590829del , CM000668.1:g.31590829del GRCh37
NC_000006.10:g.31698808del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376033.3:c.112+151del MANE Select ENSP00000365201.2:n.112+151del
ENST00000376007.8:c.112+151del ENSP00000365175.4:n.112+151del
ENST00000376033.2:c.112+151del ENSP00000365201.2:n.112+151del
ENST00000469577.5:n.136-1209del
NM_004638.3:c.112+151del NP_004629.3:n.112+151del
NM_080686.2:c.112+151del NP_542417.2:n.112+151del
XM_011514890.1:c.112+151del XP_011513192.1:n.112+151del
XM_017011274.1:c.112+151del XP_016866763.1:n.112+151del
NM_004638.4:c.112+151del MANE Select NP_004629.3:n.112+151del
NM_080686.3:c.112+151del NP_542417.2:n.112+151del
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