Canonical Allele Identifier: CA1926063606
Gene: PAPSS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727543_87727547delinsAAAAT , CM000672.2:g.87727543_87727547delinsAAAAT GRCh38
NC_000010.10:g.89487300_89487304delinsAAAAT , CM000672.1:g.89487300_89487304delinsAAAAT GRCh37
NC_000010.9:g.89477280_89477284delinsAAAAT NCBI36
NG_012150.1:g.72825_72829delinsAAAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.1086+54_1086+58delinsAAAAT MANE Select ENSP00000406157.1:n.1086+54_1086+58delinsAAAAT
ENST00000361175.8:c.1071+54_1071+58delinsAAAAT ENSP00000354436.4:n.1071+54_1071+58delinsAAAAT
ENST00000456849.1:c.1086+54_1086+58delinsAAAAT ENSP00000406157.1:n.1086+54_1086+58delinsAAAAT
NM_001015880.1:c.1086+54_1086+58delinsAAAAT NP_001015880.1:n.1086+54_1086+58delinsAAAAT
NM_004670.3:c.1071+54_1071+58delinsAAAAT NP_004661.2:n.1071+54_1071+58delinsAAAAT
NM_001015880.2:c.1086+54_1086+58delinsAAAAT MANE Select NP_001015880.1:n.1086+54_1086+58delinsAAAAT
NM_004670.4:c.1071+54_1071+58delinsAAAAT NP_004661.2:n.1071+54_1071+58delinsAAAAT