Canonical Allele Identifier: CA2610034505

Gene: PAPSS2

Linked Data

• gnomAD v4: 10-87709325-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87709325_87709326insAA , CM000672.2:g.87709325_87709326insAA	GRCh38
NC_000010.10:g.89469082_89469083insAA , CM000672.1:g.89469082_89469083insAA	GRCh37
NC_000010.9:g.89459062_89459063insAA	NCBI36
NG_012150.1:g.54607_54608insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.145+12_145+13insAA MANE Select	ENSP00000406157.1:n.145+12_145+13insAA
ENST00000361175.8:c.145+12_145+13insAA	ENSP00000354436.4:n.145+12_145+13insAA
ENST00000456849.1:c.145+12_145+13insAA	ENSP00000406157.1:n.145+12_145+13insAA
ENST00000465996.5:n.167+12_167+13insAA
ENST00000482258.1:n.188+12_188+13insAA
NM_001015880.1:c.145+12_145+13insAA	NP_001015880.1:n.145+12_145+13insAA
NM_004670.3:c.145+12_145+13insAA	NP_004661.2:n.145+12_145+13insAA
NM_001015880.2:c.145+12_145+13insAA MANE Select	NP_001015880.1:n.145+12_145+13insAA
NM_004670.4:c.145+12_145+13insAA	NP_004661.2:n.145+12_145+13insAA