Canonical Allele Identifier: CA449796912

Gene: PRRC2A

Linked Data

• MyVariant Identifiers: chr6:g.31603025A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635248A>G , CM000668.2:g.31635248A>G	GRCh38
NC_000006.11:g.31603025A>G , CM000668.1:g.31603025A>G	GRCh37
NC_000006.10:g.31711004A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5277A>G MANE Select	ENSP00000365201.2:p.Pro1759=
ENST00000376007.8:c.5277A>G	ENSP00000365175.4:p.Pro1759=
ENST00000376033.2:c.5277A>G	ENSP00000365201.2:p.Pro1759=
ENST00000469501.1:n.7A>G
ENST00000484787.1:n.688A>G
NM_004638.3:c.5277A>G	NP_004629.3:p.Pro1759=
NM_080686.2:c.5277A>G	NP_542417.2:p.Pro1759=
XM_011514890.1:c.5277A>G	XP_011513192.1:p.Pro1759=
XM_017011274.1:c.5277A>G	XP_016866763.1:p.Pro1759=
NM_004638.4:c.5277A>G MANE Select	NP_004629.3:p.Pro1759=
NM_080686.3:c.5277A>G	NP_542417.2:p.Pro1759=