Canonical Allele Identifier: CA1619235229
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622750_31622753delinsTGCC , CM000668.2:g.31622750_31622753delinsTGCC GRCh38
NC_000006.11:g.31590527_31590530delinsTGCC , CM000668.1:g.31590527_31590530delinsTGCC GRCh37
NC_000006.10:g.31698506_31698509delinsTGCC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-40_-37delinsTGCC MANE Select ENSP00000365201.2:n.-40_-37delinsTGCC
ENST00000376007.8:c.-40_-37delinsTGCC ENSP00000365175.4:n.-40_-37delinsTGCC
ENST00000376033.2:c.-40_-37delinsTGCC ENSP00000365201.2:n.-40_-37delinsTGCC
ENST00000469577.5:n.136-1511_136-1508delinsTGCC
NM_004638.3:c.-40_-37delinsTGCC NP_004629.3:n.-40_-37delinsTGCC
NM_080686.2:c.-40_-37delinsTGCC NP_542417.2:n.-40_-37delinsTGCC
XM_011514890.1:c.-40_-37delinsTGCC XP_011513192.1:n.-40_-37delinsTGCC
NM_004638.4:c.-40_-37delinsTGCC MANE Select NP_004629.3:n.-40_-37delinsTGCC
NM_080686.3:c.-40_-37delinsTGCC NP_542417.2:n.-40_-37delinsTGCC