Canonical Allele Identifier: CA2610034531

Gene: PAPSS2

Linked Data

• gnomAD v4: 10-87709347-A-ATG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87709347_87709348insTG , CM000672.2:g.87709347_87709348insTG	GRCh38
NC_000010.10:g.89469104_89469105insTG , CM000672.1:g.89469104_89469105insTG	GRCh37
NC_000010.9:g.89459084_89459085insTG	NCBI36
NG_012150.1:g.54629_54630insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.145+34_145+35insTG MANE Select	ENSP00000406157.1:n.145+34_145+35insTG
ENST00000361175.8:c.145+34_145+35insTG	ENSP00000354436.4:n.145+34_145+35insTG
ENST00000456849.1:c.145+34_145+35insTG	ENSP00000406157.1:n.145+34_145+35insTG
ENST00000465996.5:n.167+34_167+35insTG
ENST00000482258.1:n.188+34_188+35insTG
NM_001015880.1:c.145+34_145+35insTG	NP_001015880.1:n.145+34_145+35insTG
NM_004670.3:c.145+34_145+35insTG	NP_004661.2:n.145+34_145+35insTG
NM_001015880.2:c.145+34_145+35insTG MANE Select	NP_001015880.1:n.145+34_145+35insTG
NM_004670.4:c.145+34_145+35insTG	NP_004661.2:n.145+34_145+35insTG