Canonical Allele Identifier: CA2677997507

Gene: PRRC2A

Linked Data

• gnomAD v4: 6-31635064-G-GTC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635065_31635066insCT , CM000668.2:g.31635065_31635066insCT	GRCh38
NC_000006.11:g.31602842_31602843insCT , CM000668.1:g.31602842_31602843insCT	GRCh37
NC_000006.10:g.31710821_31710822insCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5161-67_5161-66insCT MANE Select	ENSP00000365201.2:n.5161-67_5161-66insCT
ENST00000376007.8:c.5161-67_5161-66insCT	ENSP00000365175.4:n.5161-67_5161-66insCT
ENST00000376033.2:c.5161-67_5161-66insCT	ENSP00000365201.2:n.5161-67_5161-66insCT
ENST00000484787.1:n.572-67_572-66insCT
NM_004638.3:c.5161-67_5161-66insCT	NP_004629.3:n.5161-67_5161-66insCT
NM_080686.2:c.5161-67_5161-66insCT	NP_542417.2:n.5161-67_5161-66insCT
XM_011514890.1:c.5161-67_5161-66insCT	XP_011513192.1:n.5161-67_5161-66insCT
XM_017011274.1:c.5161-67_5161-66insCT	XP_016866763.1:n.5161-67_5161-66insCT
NM_004638.4:c.5161-67_5161-66insCT MANE Select	NP_004629.3:n.5161-67_5161-66insCT
NM_080686.3:c.5161-67_5161-66insCT	NP_542417.2:n.5161-67_5161-66insCT