Canonical Allele Identifier: CA566690361

Gene: PRRC2A

Linked Data

• dbSNP Id: rs1261318159
• gnomAD v2: 6-31603052-C-CT
• gnomAD v4: 6-31635275-C-CT
• MyVariant Identifiers: chr6:g.31603052_31603053insT (hg19) ; chr6:g.31635275_31635276insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635276dup , CM000668.2:g.31635276dup	GRCh38
NC_000006.11:g.31603053dup , CM000668.1:g.31603053dup	GRCh37
NC_000006.10:g.31711032dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5301+4dup MANE Select	ENSP00000365201.2:n.5301+4dup
ENST00000376007.8:c.5301+4dup	ENSP00000365175.4:n.5301+4dup
ENST00000376033.2:c.5301+4dup	ENSP00000365201.2:n.5301+4dup
ENST00000469501.1:n.31+4dup
ENST00000484787.1:n.716dup
NM_004638.3:c.5301+4dup	NP_004629.3:n.5301+4dup
NM_080686.2:c.5301+4dup	NP_542417.2:n.5301+4dup
XM_011514890.1:c.5301+4dup	XP_011513192.1:n.5301+4dup
XM_017011274.1:c.5301+4dup	XP_016866763.1:n.5301+4dup
NM_004638.4:c.5301+4dup MANE Select	NP_004629.3:n.5301+4dup
NM_080686.3:c.5301+4dup	NP_542417.2:n.5301+4dup