Canonical Allele Identifier: CA2574602750
Gene: PAPSS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727530del , CM000672.2:g.87727530del GRCh38
NC_000010.10:g.89487287del , CM000672.1:g.89487287del GRCh37
NC_000010.9:g.89477267del NCBI36
NG_012150.1:g.72812del

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.1086+41del MANE Select ENSP00000406157.1:n.1086+41del
ENST00000361175.8:c.1071+41del ENSP00000354436.4:n.1071+41del
ENST00000456849.1:c.1086+41del ENSP00000406157.1:n.1086+41del
NM_001015880.1:c.1086+41del NP_001015880.1:n.1086+41del
NM_004670.3:c.1071+41del NP_004661.2:n.1071+41del
NM_001015880.2:c.1086+41del MANE Select NP_001015880.1:n.1086+41del
NM_004670.4:c.1071+41del NP_004661.2:n.1071+41del