Canonical Allele Identifier: CA1926063624

Gene: PAPSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727590_87727591delinsAT , CM000672.2:g.87727590_87727591delinsAT	GRCh38
NC_000010.10:g.89487347_89487348delinsAT , CM000672.1:g.89487347_89487348delinsAT	GRCh37
NC_000010.9:g.89477327_89477328delinsAT	NCBI36
NG_012150.1:g.72872_72873delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.1086+101_1086+102delinsAT MANE Select	ENSP00000406157.1:n.1086+101_1086+102delinsAT
ENST00000361175.8:c.1071+101_1071+102delinsAT	ENSP00000354436.4:n.1071+101_1071+102delinsAT
ENST00000456849.1:c.1086+101_1086+102delinsAT	ENSP00000406157.1:n.1086+101_1086+102delinsAT
NM_001015880.1:c.1086+101_1086+102delinsAT	NP_001015880.1:n.1086+101_1086+102delinsAT
NM_004670.3:c.1071+101_1071+102delinsAT	NP_004661.2:n.1071+101_1071+102delinsAT
NM_001015880.2:c.1086+101_1086+102delinsAT MANE Select	NP_001015880.1:n.1086+101_1086+102delinsAT
NM_004670.4:c.1071+101_1071+102delinsAT	NP_004661.2:n.1071+101_1071+102delinsAT