Canonical Allele Identifier: CA1619240647
Gene: PRRC2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31635285T= , CM000668.2:g.31635285T= GRCh38
NC_000006.11:g.31603062T= , CM000668.1:g.31603062T= GRCh37
NC_000006.10:g.31711041T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5301+13T= MANE Select ENSP00000365201.2:n.5301+13T=
ENST00000376007.8:c.5301+13T= ENSP00000365175.4:n.5301+13T=
ENST00000376033.2:c.5301+13T= ENSP00000365201.2:n.5301+13T=
ENST00000469501.1:n.31+13T=
ENST00000484787.1:n.725T=
NM_004638.3:c.5301+13T= NP_004629.3:n.5301+13T=
NM_080686.2:c.5301+13T= NP_542417.2:n.5301+13T=
XM_011514890.1:c.5301+13T= XP_011513192.1:n.5301+13T=
XM_017011274.1:c.5301+13T= XP_016866763.1:n.5301+13T=
NM_004638.4:c.5301+13T= MANE Select NP_004629.3:n.5301+13T=
NM_080686.3:c.5301+13T= NP_542417.2:n.5301+13T=
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