Canonical Allele Identifier: CA1926080732

Gene: PAPSS2

Linked Data

• dbSNP Id: rs1853669847
• gnomAD v4: 10-87727245-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727245_87727246insG , CM000672.2:g.87727245_87727246insG	GRCh38
NC_000010.10:g.89487002_89487003insG , CM000672.1:g.89487002_89487003insG	GRCh37
NC_000010.9:g.89476982_89476983insG	NCBI36
NG_012150.1:g.72527_72528insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.881-39_881-38insG MANE Select	ENSP00000406157.1:n.881-39_881-38insG
ENST00000361175.8:c.866-39_866-38insG	ENSP00000354436.4:n.866-39_866-38insG
ENST00000456849.1:c.881-39_881-38insG	ENSP00000406157.1:n.881-39_881-38insG
NM_001015880.1:c.881-39_881-38insG	NP_001015880.1:n.881-39_881-38insG
NM_004670.3:c.866-39_866-38insG	NP_004661.2:n.866-39_866-38insG
NM_001015880.2:c.881-39_881-38insG MANE Select	NP_001015880.1:n.881-39_881-38insG
NM_004670.4:c.866-39_866-38insG	NP_004661.2:n.866-39_866-38insG