Canonical Allele Identifier: CA1926080735

Gene: PAPSS2

Linked Data

• dbSNP Id: rs1853669920
• gnomAD v4: 10-87727246-ATATCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727247_87727251del , CM000672.2:g.87727247_87727251del	GRCh38
NC_000010.10:g.89487004_89487008del , CM000672.1:g.89487004_89487008del	GRCh37
NC_000010.9:g.89476984_89476988del	NCBI36
NG_012150.1:g.72529_72533del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.881-37_881-33del MANE Select	ENSP00000406157.1:n.881-37_881-33del
ENST00000361175.8:c.866-37_866-33del	ENSP00000354436.4:n.866-37_866-33del
ENST00000456849.1:c.881-37_881-33del	ENSP00000406157.1:n.881-37_881-33del
NM_001015880.1:c.881-37_881-33del	NP_001015880.1:n.881-37_881-33del
NM_004670.3:c.866-37_866-33del	NP_004661.2:n.866-37_866-33del
NM_001015880.2:c.881-37_881-33del MANE Select	NP_001015880.1:n.881-37_881-33del
NM_004670.4:c.866-37_866-33del	NP_004661.2:n.866-37_866-33del