Canonical Allele Identifier: CA2505004380
Gene: PRRC2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31634916dup , CM000668.2:g.31634916dup GRCh38
NC_000006.11:g.31602693dup , CM000668.1:g.31602693dup GRCh37
NC_000006.10:g.31710672dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5099dup MANE Select ENSP00000365201.2:p.Pro1701SerfsTer5
ENST00000376007.8:c.5099dup ENSP00000365175.4:p.Pro1701SerfsTer5
ENST00000376033.2:c.5099dup ENSP00000365201.2:p.Pro1701SerfsTer5
ENST00000484787.1:n.510dup
NM_004638.3:c.5099dup NP_004629.3:p.Pro1701SerfsTer5
NM_080686.2:c.5099dup NP_542417.2:p.Pro1701SerfsTer5
XM_011514890.1:c.5099dup XP_011513192.1:p.Pro1701SerfsTer5
XM_017011274.1:c.5099dup XP_016866763.1:p.Pro1701SerfsTer5
NM_004638.4:c.5099dup MANE Select NP_004629.3:p.Pro1701SerfsTer5
NM_080686.3:c.5099dup NP_542417.2:p.Pro1701SerfsTer5
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