Canonical Allele Identifier: CA2610038185

Gene: PAPSS2

Linked Data

• gnomAD v4: 10-87727151-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727153del , CM000672.2:g.87727153del	GRCh38
NC_000010.10:g.89486910del , CM000672.1:g.89486910del	GRCh37
NC_000010.9:g.89476890del	NCBI36
NG_012150.1:g.72435del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.881-131del MANE Select	ENSP00000406157.1:n.881-131del
ENST00000361175.8:c.866-131del	ENSP00000354436.4:n.866-131del
ENST00000456849.1:c.881-131del	ENSP00000406157.1:n.881-131del
NM_001015880.1:c.881-131del	NP_001015880.1:n.881-131del
NM_004670.3:c.866-131del	NP_004661.2:n.866-131del
NM_001015880.2:c.881-131del MANE Select	NP_001015880.1:n.881-131del
NM_004670.4:c.866-131del	NP_004661.2:n.866-131del