Canonical Allele Identifier: CA3716613

Gene: PRRC2A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31636267T>G , CM000668.2:g.31636267T>G	GRCh38
NC_000006.11:g.31604044T>G , CM000668.1:g.31604044T>G	GRCh37
NC_000006.10:g.31712023T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5683T>G MANE Select	ENSP00000365201.2:p.Leu1895Val
ENST00000376007.8:c.5683T>G	ENSP00000365175.4:p.Leu1895Val
ENST00000376033.2:c.5683T>G	ENSP00000365201.2:p.Leu1895Val
ENST00000487839.1:n.617T>G
ENST00000492691.5:n.21T>G
NM_004638.3:c.5683T>G	NP_004629.3:p.Leu1895Val
NM_080686.2:c.5683T>G	NP_542417.2:p.Leu1895Val
XM_011514890.1:c.5683T>G	XP_011513192.1:p.Leu1895Val
XM_017011274.1:c.5683T>G	XP_016866763.1:p.Leu1895Val
NM_004638.4:c.5683T>G MANE Select	NP_004629.3:p.Leu1895Val
NM_080686.3:c.5683T>G	NP_542417.2:p.Leu1895Val