Canonical Allele Identifier: CA363331138
Gene: PRRC2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31590592C>A (hg19) chr6:g.31622815C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622815C>A , CM000668.2:g.31622815C>A GRCh38
NC_000006.11:g.31590592C>A , CM000668.1:g.31590592C>A GRCh37
NC_000006.10:g.31698571C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000706625.1:c.42C>A ENSP00000516471.1:p.Cys14Ter
ENST00000376033.3:c.26C>A MANE Select ENSP00000365201.2:p.Ala9Asp
ENST00000376007.8:c.26C>A ENSP00000365175.4:p.Ala9Asp
ENST00000376033.2:c.26C>A ENSP00000365201.2:p.Ala9Asp
ENST00000469577.5:n.136-1446C>A
NM_004638.3:c.26C>A NP_004629.3:p.Ala9Asp
NM_080686.2:c.26C>A NP_542417.2:p.Ala9Asp
XM_011514890.1:c.26C>A XP_011513192.1:p.Ala9Asp
XM_017011274.1:c.26C>A XP_016866763.1:p.Ala9Asp
NM_004638.4:c.26C>A MANE Select NP_004629.3:p.Ala9Asp
NM_080686.3:c.26C>A NP_542417.2:p.Ala9Asp
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