Canonical Allele Identifier: CA1619235543

Gene: PRRC2A

Linked Data

• dbSNP Id: rs1775471353

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31623027del , CM000668.2:g.31623027del	GRCh38
NC_000006.11:g.31590804del , CM000668.1:g.31590804del	GRCh37
NC_000006.10:g.31698783del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.112+126del MANE Select	ENSP00000365201.2:n.112+126del
ENST00000376007.8:c.112+126del	ENSP00000365175.4:n.112+126del
ENST00000376033.2:c.112+126del	ENSP00000365201.2:n.112+126del
ENST00000469577.5:n.136-1234del
NM_004638.3:c.112+126del	NP_004629.3:n.112+126del
NM_080686.2:c.112+126del	NP_542417.2:n.112+126del
XM_011514890.1:c.112+126del	XP_011513192.1:n.112+126del
XM_017011274.1:c.112+126del	XP_016866763.1:n.112+126del
NM_004638.4:c.112+126del MANE Select	NP_004629.3:n.112+126del
NM_080686.3:c.112+126del	NP_542417.2:n.112+126del