Canonical Allele Identifier: CA823901177

Gene: PRRC2A

Linked Data

• dbSNP Id: rs1323391087
• gnomAD v3: 6-31634987-C-CA
• gnomAD v4: 6-31634987-C-CA
• MyVariant Identifiers: chr6:g.31602764_31602765insA (hg19) ; chr6:g.31634987_31634988insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31634993dup , CM000668.2:g.31634993dup	GRCh38
NC_000006.11:g.31602770dup , CM000668.1:g.31602770dup	GRCh37
NC_000006.10:g.31710749dup	NCBI36

Transcript Alleles

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