Canonical Allele Identifier: CA3716436

Gene: PRRC2A

Linked Data

• dbSNP Id: rs774424168
• ExAC: 6:31602911 GCTGCCCCGGGAGCAGCCT / G
• gnomAD v2: 6-31602911-GCTGCCCCGGGAGCAGCCT-G
• gnomAD v4: 6-31635134-GCTGCCCCGGGAGCAGCCT-G
• MyVariant Identifiers: chr6:g.31602912_31602929del (hg19) ; chr6:g.31635135_31635152del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635142_31635159del , CM000668.2:g.31635142_31635159del	GRCh38
NC_000006.11:g.31602919_31602936del , CM000668.1:g.31602919_31602936del	GRCh37
NC_000006.10:g.31710898_31710915del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5171_5188del MANE Select	ENSP00000365201.2:p.Arg1724_Pro1729del
ENST00000376007.8:c.5171_5188del	ENSP00000365175.4:p.Arg1724_Pro1729del
ENST00000376033.2:c.5171_5188del	ENSP00000365201.2:p.Arg1724_Pro1729del
ENST00000484787.1:n.582_599del
NM_004638.3:c.5171_5188del	NP_004629.3:p.Arg1724_Pro1729del
NM_080686.2:c.5171_5188del	NP_542417.2:p.Arg1724_Pro1729del
XM_011514890.1:c.5171_5188del	XP_011513192.1:p.Arg1724_Pro1729del
XM_017011274.1:c.5171_5188del	XP_016866763.1:p.Arg1724_Pro1729del
NM_004638.4:c.5171_5188del MANE Select	NP_004629.3:p.Arg1724_Pro1729del
NM_080686.3:c.5171_5188del	NP_542417.2:p.Arg1724_Pro1729del