Canonical Allele Identifier: CA2578566263
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31635275C>G , CM000668.2:g.31635275C>G GRCh38
NC_000006.11:g.31603052C>G , CM000668.1:g.31603052C>G GRCh37
NC_000006.10:g.31711031C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5301+3C>G MANE Select ENSP00000365201.2:n.5301+3C>G
ENST00000376007.8:c.5301+3C>G ENSP00000365175.4:n.5301+3C>G
ENST00000376033.2:c.5301+3C>G ENSP00000365201.2:n.5301+3C>G
ENST00000469501.1:n.31+3C>G
ENST00000484787.1:n.715C>G
NM_004638.3:c.5301+3C>G NP_004629.3:n.5301+3C>G
NM_080686.2:c.5301+3C>G NP_542417.2:n.5301+3C>G
XM_011514890.1:c.5301+3C>G XP_011513192.1:n.5301+3C>G
XM_017011274.1:c.5301+3C>G XP_016866763.1:n.5301+3C>G
NM_004638.4:c.5301+3C>G MANE Select NP_004629.3:n.5301+3C>G
NM_080686.3:c.5301+3C>G NP_542417.2:n.5301+3C>G