Canonical Allele Identifier: CA2677997567

Gene: PRRC2A

Linked Data

• gnomAD v4: 6-31635142-G-GGGAGCAGCCTCTGCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635143_31635160dup , CM000668.2:g.31635143_31635160dup	GRCh38
NC_000006.11:g.31602920_31602937dup , CM000668.1:g.31602920_31602937dup	GRCh37
NC_000006.10:g.31710899_31710916dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5172_5189dup MANE Select	ENSP00000365201.2:p.Pro1730_Gly1731insGluGlnProLeuProPro
ENST00000376007.8:c.5172_5189dup	ENSP00000365175.4:p.Pro1730_Gly1731insGluGlnProLeuProPro
ENST00000376033.2:c.5172_5189dup	ENSP00000365201.2:p.Pro1730_Gly1731insGluGlnProLeuProPro
ENST00000484787.1:n.583_600dup
NM_004638.3:c.5172_5189dup	NP_004629.3:p.Pro1730_Gly1731insGluGlnProLeuProPro
NM_080686.2:c.5172_5189dup	NP_542417.2:p.Pro1730_Gly1731insGluGlnProLeuProPro
XM_011514890.1:c.5172_5189dup	XP_011513192.1:p.Pro1730_Gly1731insGluGlnProLeuProPro
XM_017011274.1:c.5172_5189dup	XP_016866763.1:p.Pro1730_Gly1731insGluGlnProLeuProPro
NM_004638.4:c.5172_5189dup MANE Select	NP_004629.3:p.Pro1730_Gly1731insGluGlnProLeuProPro
NM_080686.3:c.5172_5189dup	NP_542417.2:p.Pro1730_Gly1731insGluGlnProLeuProPro