Canonical Allele Identifier: CA2594637020

Gene: PRRC2A

Linked Data

• gnomAD v3: 6-31635057-C-CGT
• gnomAD v4: 6-31635057-C-CGT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635064_31635065dup , CM000668.2:g.31635064_31635065dup	GRCh38
NC_000006.11:g.31602841_31602842dup , CM000668.1:g.31602841_31602842dup	GRCh37
NC_000006.10:g.31710820_31710821dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5161-68_5161-67dup MANE Select	ENSP00000365201.2:n.5161-68_5161-67dup
ENST00000376007.8:c.5161-68_5161-67dup	ENSP00000365175.4:n.5161-68_5161-67dup
ENST00000376033.2:c.5161-68_5161-67dup	ENSP00000365201.2:n.5161-68_5161-67dup
ENST00000484787.1:n.572-68_572-67dup
NM_004638.3:c.5161-68_5161-67dup	NP_004629.3:n.5161-68_5161-67dup
NM_080686.2:c.5161-68_5161-67dup	NP_542417.2:n.5161-68_5161-67dup
XM_011514890.1:c.5161-68_5161-67dup	XP_011513192.1:n.5161-68_5161-67dup
XM_017011274.1:c.5161-68_5161-67dup	XP_016866763.1:n.5161-68_5161-67dup
NM_004638.4:c.5161-68_5161-67dup MANE Select	NP_004629.3:n.5161-68_5161-67dup
NM_080686.3:c.5161-68_5161-67dup	NP_542417.2:n.5161-68_5161-67dup