Canonical Allele Identifier: CA136867873
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs35201773

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31635268A>T , CM000668.2:g.31635268A>T GRCh38
NC_000006.11:g.31603045A>T , CM000668.1:g.31603045A>T GRCh37
NC_000006.10:g.31711024A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5297A>T MANE Select ENSP00000365201.2:p.Asp1766Val
ENST00000376007.8:c.5297A>T ENSP00000365175.4:p.Asp1766Val
ENST00000376033.2:c.5297A>T ENSP00000365201.2:p.Asp1766Val
ENST00000469501.1:n.27A>T
ENST00000484787.1:n.708A>T
NM_004638.3:c.5297A>T NP_004629.3:p.Asp1766Val
NM_080686.2:c.5297A>T NP_542417.2:p.Asp1766Val
XM_011514890.1:c.5297A>T XP_011513192.1:p.Asp1766Val
XM_017011274.1:c.5297A>T XP_016866763.1:p.Asp1766Val
NM_004638.4:c.5297A>T MANE Select NP_004629.3:p.Asp1766Val
NM_080686.3:c.5297A>T NP_542417.2:p.Asp1766Val