Canonical Allele Identifier: CA1926063553

Gene: PAPSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727438A= , CM000672.2:g.87727438A=	GRCh38
NC_000010.10:g.89487195A= , CM000672.1:g.89487195A=	GRCh37
NC_000010.9:g.89477175A=	NCBI36
NG_012150.1:g.72720A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.1035A= MANE Select	ENSP00000406157.1:p.Glu345=
ENST00000361175.8:c.1020A=	ENSP00000354436.4:p.Glu340=
ENST00000456849.1:c.1035A=	ENSP00000406157.1:p.Glu345=
NM_001015880.1:c.1035A=	NP_001015880.1:p.Glu345=
NM_004670.3:c.1020A=	NP_004661.2:p.Glu340=
NM_001015880.2:c.1035A= MANE Select	NP_001015880.1:p.Glu345=
NM_004670.4:c.1020A=	NP_004661.2:p.Glu340=