Canonical Allele Identifier: CA136852610

Gene: PRRC2A

Linked Data

• dbSNP Id: rs753357550
• gnomAD v3: 6-31623011-AGAG-A
• gnomAD v4: 6-31623011-AGAG-A
• MyVariant Identifiers: chr6:g.31590789_31590791del (hg19) ; chr6:g.31623012_31623014del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31623015_31623017del , CM000668.2:g.31623015_31623017del	GRCh38
NC_000006.11:g.31590792_31590794del , CM000668.1:g.31590792_31590794del	GRCh37
NC_000006.10:g.31698771_31698773del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.112+114_112+116del MANE Select	ENSP00000365201.2:n.112+114_112+116del
ENST00000376007.8:c.112+114_112+116del	ENSP00000365175.4:n.112+114_112+116del
ENST00000376033.2:c.112+114_112+116del	ENSP00000365201.2:n.112+114_112+116del
ENST00000469577.5:n.136-1246_136-1244del
NM_004638.3:c.112+114_112+116del	NP_004629.3:n.112+114_112+116del
NM_080686.2:c.112+114_112+116del	NP_542417.2:n.112+114_112+116del
XM_011514890.1:c.112+114_112+116del	XP_011513192.1:n.112+114_112+116del
XM_017011274.1:c.112+114_112+116del	XP_016866763.1:n.112+114_112+116del
NM_004638.4:c.112+114_112+116del MANE Select	NP_004629.3:n.112+114_112+116del
NM_080686.3:c.112+114_112+116del	NP_542417.2:n.112+114_112+116del