Canonical Allele Identifier: CA363331244

Gene: PRRC2A

Linked Data

• gnomAD v4: 6-31622821-G-A
• MyVariant Identifiers: chr6:g.31590598G>A (hg19) ; chr6:g.31622821G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31622821G>A , CM000668.2:g.31622821G>A	GRCh38
NC_000006.11:g.31590598G>A , CM000668.1:g.31590598G>A	GRCh37
NC_000006.10:g.31698577G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706625.1:c.48G>A	ENSP00000516471.1:p.Gly16=
ENST00000376033.3:c.32G>A MANE Select	ENSP00000365201.2:p.Gly11Glu
ENST00000376007.8:c.32G>A	ENSP00000365175.4:p.Gly11Glu
ENST00000376033.2:c.32G>A	ENSP00000365201.2:p.Gly11Glu
ENST00000469577.5:n.136-1440G>A
NM_004638.3:c.32G>A	NP_004629.3:p.Gly11Glu
NM_080686.2:c.32G>A	NP_542417.2:p.Gly11Glu
XM_011514890.1:c.32G>A	XP_011513192.1:p.Gly11Glu
XM_017011274.1:c.32G>A	XP_016866763.1:p.Gly11Glu
NM_004638.4:c.32G>A MANE Select	NP_004629.3:p.Gly11Glu
NM_080686.3:c.32G>A	NP_542417.2:p.Gly11Glu