Canonical Allele Identifier: CA566355385

Gene: PRRC2A

Linked Data

• dbSNP Id: rs1561791088
• gnomAD v2: 6-31590519-GGGGGA-G
• MyVariant Identifiers: chr6:g.31590520_31590524del (hg19) ; chr6:g.31622743_31622747del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31622745_31622749del , CM000668.2:g.31622745_31622749del	GRCh38
NC_000006.11:g.31590522_31590526del , CM000668.1:g.31590522_31590526del	GRCh37
NC_000006.10:g.31698501_31698505del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.-45_-41del MANE Select	ENSP00000365201.2:n.-45_-41del
ENST00000376007.8:c.-45_-41del	ENSP00000365175.4:n.-45_-41del
ENST00000376033.2:c.-45_-41del	ENSP00000365201.2:n.-45_-41del
ENST00000469577.5:n.136-1516_136-1512del
NM_004638.3:c.-45_-41del	NP_004629.3:n.-45_-41del
NM_080686.2:c.-45_-41del	NP_542417.2:n.-45_-41del
XM_011514890.1:c.-45_-41del	XP_011513192.1:n.-45_-41del
NM_004638.4:c.-45_-41del MANE Select	NP_004629.3:n.-45_-41del
NM_080686.3:c.-45_-41del	NP_542417.2:n.-45_-41del