Canonical Allele Identifier: CA566690420

Gene: PRRC2A

Linked Data

• dbSNP Id: rs1335072253
• gnomAD v2: 6-31602871-T-TCC
• gnomAD v4: 6-31635094-T-TCC
• MyVariant Identifiers: chr6:g.31602871_31602872insCC (hg19) ; chr6:g.31635094_31635095insCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635096_31635097dup , CM000668.2:g.31635096_31635097dup	GRCh38
NC_000006.11:g.31602873_31602874dup , CM000668.1:g.31602873_31602874dup	GRCh37
NC_000006.10:g.31710852_31710853dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376033.3:c.5161-36_5161-35dup MANE Select	ENSP00000365201.2:n.5161-36_5161-35dup
ENST00000376007.8:c.5161-36_5161-35dup	ENSP00000365175.4:n.5161-36_5161-35dup
ENST00000376033.2:c.5161-36_5161-35dup	ENSP00000365201.2:n.5161-36_5161-35dup
ENST00000484787.1:n.572-36_572-35dup
NM_004638.3:c.5161-36_5161-35dup	NP_004629.3:n.5161-36_5161-35dup
NM_080686.2:c.5161-36_5161-35dup	NP_542417.2:n.5161-36_5161-35dup
XM_011514890.1:c.5161-36_5161-35dup	XP_011513192.1:n.5161-36_5161-35dup
XM_017011274.1:c.5161-36_5161-35dup	XP_016866763.1:n.5161-36_5161-35dup
NM_004638.4:c.5161-36_5161-35dup MANE Select	NP_004629.3:n.5161-36_5161-35dup
NM_080686.3:c.5161-36_5161-35dup	NP_542417.2:n.5161-36_5161-35dup