Canonical Allele Identifier: CA2578565761
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622779C>A , CM000668.2:g.31622779C>A GRCh38
NC_000006.11:g.31590556C>A , CM000668.1:g.31590556C>A GRCh37
NC_000006.10:g.31698535C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000706625.1:c.6C>A ENSP00000516471.1:p.Ser2Arg
ENST00000376033.3:c.-11C>A MANE Select ENSP00000365201.2:n.-11C>A
ENST00000376007.8:c.-11C>A ENSP00000365175.4:n.-11C>A
ENST00000376033.2:c.-11C>A ENSP00000365201.2:n.-11C>A
ENST00000469577.5:n.136-1482C>A
NM_004638.3:c.-11C>A NP_004629.3:n.-11C>A
NM_080686.2:c.-11C>A NP_542417.2:n.-11C>A
XM_011514890.1:c.-11C>A XP_011513192.1:n.-11C>A
NM_004638.4:c.-11C>A MANE Select NP_004629.3:n.-11C>A
NM_080686.3:c.-11C>A NP_542417.2:n.-11C>A