Canonical Allele Identifier: CA2677997412

Gene: PRRC2A

Linked Data

• gnomAD v4: 6-31634987-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31634992_31634993del , CM000668.2:g.31634992_31634993del	GRCh38
NC_000006.11:g.31602769_31602770del , CM000668.1:g.31602769_31602770del	GRCh37
NC_000006.10:g.31710748_31710749del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5160+15_5160+16del MANE Select	ENSP00000365201.2:n.5160+15_5160+16del
ENST00000376007.8:c.5160+15_5160+16del	ENSP00000365175.4:n.5160+15_5160+16del
ENST00000376033.2:c.5160+15_5160+16del	ENSP00000365201.2:n.5160+15_5160+16del
ENST00000484787.1:n.571+15_571+16del
NM_004638.3:c.5160+15_5160+16del	NP_004629.3:n.5160+15_5160+16del
NM_080686.2:c.5160+15_5160+16del	NP_542417.2:n.5160+15_5160+16del
XM_011514890.1:c.5160+15_5160+16del	XP_011513192.1:n.5160+15_5160+16del
XM_017011274.1:c.5160+15_5160+16del	XP_016866763.1:n.5160+15_5160+16del
NM_004638.4:c.5160+15_5160+16del MANE Select	NP_004629.3:n.5160+15_5160+16del
NM_080686.3:c.5160+15_5160+16del	NP_542417.2:n.5160+15_5160+16del