Canonical Allele Identifier: CA363331989
Gene: PRRC2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622869A>G , CM000668.2:g.31622869A>G GRCh38
NC_000006.11:g.31590646A>G , CM000668.1:g.31590646A>G GRCh37
NC_000006.10:g.31698625A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.80A>G MANE Select ENSP00000365201.2:p.Lys27Arg
ENST00000376007.8:c.80A>G ENSP00000365175.4:p.Lys27Arg
ENST00000376033.2:c.80A>G ENSP00000365201.2:p.Lys27Arg
ENST00000469577.5:n.136-1392A>G
NM_004638.3:c.80A>G NP_004629.3:p.Lys27Arg
NM_080686.2:c.80A>G NP_542417.2:p.Lys27Arg
XM_011514890.1:c.80A>G XP_011513192.1:p.Lys27Arg
XM_017011274.1:c.80A>G XP_016866763.1:p.Lys27Arg
NM_004638.4:c.80A>G MANE Select NP_004629.3:p.Lys27Arg
NM_080686.3:c.80A>G NP_542417.2:p.Lys27Arg