Canonical Allele Identifier: CA363332123
Gene: PRRC2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622890A>G , CM000668.2:g.31622890A>G GRCh38
NC_000006.11:g.31590667A>G , CM000668.1:g.31590667A>G GRCh37
NC_000006.10:g.31698646A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.101A>G MANE Select ENSP00000365201.2:p.Gln34Arg
ENST00000376007.8:c.101A>G ENSP00000365175.4:p.Gln34Arg
ENST00000376033.2:c.101A>G ENSP00000365201.2:p.Gln34Arg
ENST00000469577.5:n.136-1371A>G
NM_004638.3:c.101A>G NP_004629.3:p.Gln34Arg
NM_080686.2:c.101A>G NP_542417.2:p.Gln34Arg
XM_011514890.1:c.101A>G XP_011513192.1:p.Gln34Arg
XM_017011274.1:c.101A>G XP_016866763.1:p.Gln34Arg
NM_004638.4:c.101A>G MANE Select NP_004629.3:p.Gln34Arg
NM_080686.3:c.101A>G NP_542417.2:p.Gln34Arg