Canonical Allele Identifier: CA1926073282

Gene: PAPSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87709214A= , CM000672.2:g.87709214A=	GRCh38
NC_000010.10:g.89468971A= , CM000672.1:g.89468971A=	GRCh37
NC_000010.9:g.89458951A=	NCBI36
NG_012150.1:g.54496A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000456849.2:c.46A= MANE Select	ENSP00000406157.1:p.Thr16=
ENST00000361175.8:c.46A=	ENSP00000354436.4:p.Thr16=
ENST00000456849.1:c.46A=	ENSP00000406157.1:p.Thr16=
ENST00000465996.5:n.68A=
ENST00000482258.1:n.89A=
NM_001015880.1:c.46A=	NP_001015880.1:p.Thr16=
NM_004670.3:c.46A=	NP_004661.2:p.Thr16=
NM_001015880.2:c.46A= MANE Select	NP_001015880.1:p.Thr16=
NM_004670.4:c.46A=	NP_004661.2:p.Thr16=