Canonical Allele Identifier: CA1926063609

Gene: PAPSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727549_87727551delinsACT , CM000672.2:g.87727549_87727551delinsACT	GRCh38
NC_000010.10:g.89487306_89487308delinsACT , CM000672.1:g.89487306_89487308delinsACT	GRCh37
NC_000010.9:g.89477286_89477288delinsACT	NCBI36
NG_012150.1:g.72831_72833delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.1086+60_1086+62delinsACT MANE Select	ENSP00000406157.1:n.1086+60_1086+62delinsACT
ENST00000361175.8:c.1071+60_1071+62delinsACT	ENSP00000354436.4:n.1071+60_1071+62delinsACT
ENST00000456849.1:c.1086+60_1086+62delinsACT	ENSP00000406157.1:n.1086+60_1086+62delinsACT
NM_001015880.1:c.1086+60_1086+62delinsACT	NP_001015880.1:n.1086+60_1086+62delinsACT
NM_004670.3:c.1071+60_1071+62delinsACT	NP_004661.2:n.1071+60_1071+62delinsACT
NM_001015880.2:c.1086+60_1086+62delinsACT MANE Select	NP_001015880.1:n.1086+60_1086+62delinsACT
NM_004670.4:c.1071+60_1071+62delinsACT	NP_004661.2:n.1071+60_1071+62delinsACT