Canonical Allele Identifier: CA363362127
Gene: PRRC2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31634880G>T , CM000668.2:g.31634880G>T GRCh38
NC_000006.11:g.31602657G>T , CM000668.1:g.31602657G>T GRCh37
NC_000006.10:g.31710636G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5063G>T MANE Select ENSP00000365201.2:p.Gly1688Val
ENST00000376007.8:c.5063G>T ENSP00000365175.4:p.Gly1688Val
ENST00000376033.2:c.5063G>T ENSP00000365201.2:p.Gly1688Val
ENST00000484787.1:n.474G>T
NM_004638.3:c.5063G>T NP_004629.3:p.Gly1688Val
NM_080686.2:c.5063G>T NP_542417.2:p.Gly1688Val
XM_011514890.1:c.5063G>T XP_011513192.1:p.Gly1688Val
XM_017011274.1:c.5063G>T XP_016866763.1:p.Gly1688Val
NM_004638.4:c.5063G>T MANE Select NP_004629.3:p.Gly1688Val
NM_080686.3:c.5063G>T NP_542417.2:p.Gly1688Val