Canonical Allele Identifier: CA363331643
Gene: PRRC2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622844T>A , CM000668.2:g.31622844T>A GRCh38
NC_000006.11:g.31590621T>A , CM000668.1:g.31590621T>A GRCh37
NC_000006.10:g.31698600T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000706625.1:c.71T>A ENSP00000516471.1:p.Leu24His
ENST00000376033.3:c.55T>A MANE Select ENSP00000365201.2:p.Ser19Thr
ENST00000376007.8:c.55T>A ENSP00000365175.4:p.Ser19Thr
ENST00000376033.2:c.55T>A ENSP00000365201.2:p.Ser19Thr
ENST00000469577.5:n.136-1417T>A
NM_004638.3:c.55T>A NP_004629.3:p.Ser19Thr
NM_080686.2:c.55T>A NP_542417.2:p.Ser19Thr
XM_011514890.1:c.55T>A XP_011513192.1:p.Ser19Thr
XM_017011274.1:c.55T>A XP_016866763.1:p.Ser19Thr
NM_004638.4:c.55T>A MANE Select NP_004629.3:p.Ser19Thr
NM_080686.3:c.55T>A NP_542417.2:p.Ser19Thr