Canonical Allele Identifier: CA1619240546
Gene: PRRC2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31635088T= , CM000668.2:g.31635088T= GRCh38
NC_000006.11:g.31602865T= , CM000668.1:g.31602865T= GRCh37
NC_000006.10:g.31710844T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5161-44T= MANE Select ENSP00000365201.2:n.5161-44T=
ENST00000376007.8:c.5161-44T= ENSP00000365175.4:n.5161-44T=
ENST00000376033.2:c.5161-44T= ENSP00000365201.2:n.5161-44T=
ENST00000484787.1:n.572-44T=
NM_004638.3:c.5161-44T= NP_004629.3:n.5161-44T=
NM_080686.2:c.5161-44T= NP_542417.2:n.5161-44T=
XM_011514890.1:c.5161-44T= XP_011513192.1:n.5161-44T=
XM_017011274.1:c.5161-44T= XP_016866763.1:n.5161-44T=
NM_004638.4:c.5161-44T= MANE Select NP_004629.3:n.5161-44T=
NM_080686.3:c.5161-44T= NP_542417.2:n.5161-44T=
Search 100 bp 5'
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