Canonical Allele Identifier: CA2677997109
Gene: PRRC2A HGNC NCBI

Linked Data

gnomAD v4: 6-31622974-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622974T>A , CM000668.2:g.31622974T>A GRCh38
NC_000006.11:g.31590751T>A , CM000668.1:g.31590751T>A GRCh37
NC_000006.10:g.31698730T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.112+73T>A MANE Select ENSP00000365201.2:n.112+73T>A
ENST00000376007.8:c.112+73T>A ENSP00000365175.4:n.112+73T>A
ENST00000376033.2:c.112+73T>A ENSP00000365201.2:n.112+73T>A
ENST00000469577.5:n.136-1287T>A
NM_004638.3:c.112+73T>A NP_004629.3:n.112+73T>A
NM_080686.2:c.112+73T>A NP_542417.2:n.112+73T>A
XM_011514890.1:c.112+73T>A XP_011513192.1:n.112+73T>A
XM_017011274.1:c.112+73T>A XP_016866763.1:n.112+73T>A
NM_004638.4:c.112+73T>A MANE Select NP_004629.3:n.112+73T>A
NM_080686.3:c.112+73T>A NP_542417.2:n.112+73T>A
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