Canonical Allele Identifier: CA1926073332

Gene: PAPSS2

Linked Data

• dbSNP Id: rs72025574
• gnomAD v4: 10-87709326-C-CATATATAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87709338_87709345dup , CM000672.2:g.87709338_87709345dup	GRCh38
NC_000010.10:g.89469095_89469102dup , CM000672.1:g.89469095_89469102dup	GRCh37
NC_000010.9:g.89459075_89459082dup	NCBI36
NG_012150.1:g.54620_54627dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.145+25_145+32dup MANE Select	ENSP00000406157.1:n.145+25_145+32dup
ENST00000361175.8:c.145+25_145+32dup	ENSP00000354436.4:n.145+25_145+32dup
ENST00000456849.1:c.145+25_145+32dup	ENSP00000406157.1:n.145+25_145+32dup
ENST00000465996.5:n.167+25_167+32dup
ENST00000482258.1:n.188+25_188+32dup
NM_001015880.1:c.145+25_145+32dup	NP_001015880.1:n.145+25_145+32dup
NM_004670.3:c.145+25_145+32dup	NP_004661.2:n.145+25_145+32dup
NM_001015880.2:c.145+25_145+32dup MANE Select	NP_001015880.1:n.145+25_145+32dup
NM_004670.4:c.145+25_145+32dup	NP_004661.2:n.145+25_145+32dup