Canonical Allele Identifier: CA1926073317

Gene: PAPSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87709298A= , CM000672.2:g.87709298A=	GRCh38
NC_000010.10:g.89469055A= , CM000672.1:g.89469055A=	GRCh37
NC_000010.9:g.89459035A=	NCBI36
NG_012150.1:g.54580A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.130A= MANE Select	ENSP00000406157.1:p.Thr44=
ENST00000361175.8:c.130A=	ENSP00000354436.4:p.Thr44=
ENST00000456849.1:c.130A=	ENSP00000406157.1:p.Thr44=
ENST00000465996.5:n.152A=
ENST00000482258.1:n.173A=
NM_001015880.1:c.130A=	NP_001015880.1:p.Thr44=
NM_004670.3:c.130A=	NP_004661.2:p.Thr44=
NM_001015880.2:c.130A= MANE Select	NP_001015880.1:p.Thr44=
NM_004670.4:c.130A=	NP_004661.2:p.Thr44=