Canonical Allele Identifier: CA449662001

Gene: PRRC2A

Linked Data

• MyVariant Identifiers: chr6:g.31590677T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31622900T>G , CM000668.2:g.31622900T>G	GRCh38
NC_000006.11:g.31590677T>G , CM000668.1:g.31590677T>G	GRCh37
NC_000006.10:g.31698656T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.111T>G MANE Select	ENSP00000365201.2:p.Ala37=
ENST00000376007.8:c.111T>G	ENSP00000365175.4:p.Ala37=
ENST00000376033.2:c.111T>G	ENSP00000365201.2:p.Ala37=
ENST00000469577.5:n.136-1361T>G
NM_004638.3:c.111T>G	NP_004629.3:p.Ala37=
NM_080686.2:c.111T>G	NP_542417.2:p.Ala37=
XM_011514890.1:c.111T>G	XP_011513192.1:p.Ala37=
XM_017011274.1:c.111T>G	XP_016866763.1:p.Ala37=
NM_004638.4:c.111T>G MANE Select	NP_004629.3:p.Ala37=
NM_080686.3:c.111T>G	NP_542417.2:p.Ala37=