Canonical Allele Identifier: CA566690402

Gene: PRRC2A

Linked Data

• dbSNP Id: rs1561837817
• gnomAD v2: 6-31602784-GT-G
• gnomAD v4: 6-31635007-GT-G
• MyVariant Identifiers: chr6:g.31602785del (hg19) ; chr6:g.31635008del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635010del , CM000668.2:g.31635010del	GRCh38
NC_000006.11:g.31602787del , CM000668.1:g.31602787del	GRCh37
NC_000006.10:g.31710766del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5160+33del MANE Select	ENSP00000365201.2:n.5160+33del
ENST00000376007.8:c.5160+33del	ENSP00000365175.4:n.5160+33del
ENST00000376033.2:c.5160+33del	ENSP00000365201.2:n.5160+33del
ENST00000484787.1:n.571+33del
NM_004638.3:c.5160+33del	NP_004629.3:n.5160+33del
NM_080686.2:c.5160+33del	NP_542417.2:n.5160+33del
XM_011514890.1:c.5160+33del	XP_011513192.1:n.5160+33del
XM_017011274.1:c.5160+33del	XP_016866763.1:n.5160+33del
NM_004638.4:c.5160+33del MANE Select	NP_004629.3:n.5160+33del
NM_080686.3:c.5160+33del	NP_542417.2:n.5160+33del