Canonical Allele Identifier: CA1619235209
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622741_31622742delinsTG , CM000668.2:g.31622741_31622742delinsTG GRCh38
NC_000006.11:g.31590518_31590519delinsTG , CM000668.1:g.31590518_31590519delinsTG GRCh37
NC_000006.10:g.31698497_31698498delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-49_-48delinsTG MANE Select ENSP00000365201.2:n.-49_-48delinsTG
ENST00000376007.8:c.-49_-48delinsTG ENSP00000365175.4:n.-49_-48delinsTG
ENST00000376033.2:c.-49_-48delinsTG ENSP00000365201.2:n.-49_-48delinsTG
ENST00000469577.5:n.136-1520_136-1519delinsTG
NM_004638.3:c.-49_-48delinsTG NP_004629.3:n.-49_-48delinsTG
NM_080686.2:c.-49_-48delinsTG NP_542417.2:n.-49_-48delinsTG
XM_011514890.1:c.-49_-48delinsTG XP_011513192.1:n.-49_-48delinsTG
NM_004638.4:c.-49_-48delinsTG MANE Select NP_004629.3:n.-49_-48delinsTG
NM_080686.3:c.-49_-48delinsTG NP_542417.2:n.-49_-48delinsTG