Canonical Allele Identifier: CA2677999681

Gene: PRRC2A

Linked Data

• gnomAD v4: 6-31637418-CACTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31637419_31637422del , CM000668.2:g.31637419_31637422del	GRCh38
NC_000006.11:g.31605196_31605199del , CM000668.1:g.31605196_31605199del	GRCh37
NC_000006.10:g.31713175_31713178del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.6334-27_6334-24del MANE Select	ENSP00000365201.2:n.6334-27_6334-24del
ENST00000376007.8:c.6334-27_6334-24del	ENSP00000365175.4:n.6334-27_6334-24del
ENST00000376033.2:c.6334-27_6334-24del	ENSP00000365201.2:n.6334-27_6334-24del
ENST00000462617.1:n.663_666del
ENST00000482441.1:n.394-27_394-24del
ENST00000492691.5:n.766_769del
NM_004638.3:c.6334-27_6334-24del	NP_004629.3:n.6334-27_6334-24del
NM_080686.2:c.6334-27_6334-24del	NP_542417.2:n.6334-27_6334-24del
XM_011514890.1:c.6121-27_6121-24del	XP_011513192.1:n.6121-27_6121-24del
XM_017011274.1:c.6121-27_6121-24del	XP_016866763.1:n.6121-27_6121-24del
NM_004638.4:c.6334-27_6334-24del MANE Select	NP_004629.3:n.6334-27_6334-24del
NM_080686.3:c.6334-27_6334-24del	NP_542417.2:n.6334-27_6334-24del