Canonical Allele Identifier: CA2610034525

Gene: PAPSS2

Linked Data

• gnomAD v4: 10-87709344-T-TGA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87709344_87709345insGA , CM000672.2:g.87709344_87709345insGA	GRCh38
NC_000010.10:g.89469101_89469102insGA , CM000672.1:g.89469101_89469102insGA	GRCh37
NC_000010.9:g.89459081_89459082insGA	NCBI36
NG_012150.1:g.54626_54627insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.145+31_145+32insGA MANE Select	ENSP00000406157.1:n.145+31_145+32insGA
ENST00000361175.8:c.145+31_145+32insGA	ENSP00000354436.4:n.145+31_145+32insGA
ENST00000456849.1:c.145+31_145+32insGA	ENSP00000406157.1:n.145+31_145+32insGA
ENST00000465996.5:n.167+31_167+32insGA
ENST00000482258.1:n.188+31_188+32insGA
NM_001015880.1:c.145+31_145+32insGA	NP_001015880.1:n.145+31_145+32insGA
NM_004670.3:c.145+31_145+32insGA	NP_004661.2:n.145+31_145+32insGA
NM_001015880.2:c.145+31_145+32insGA MANE Select	NP_001015880.1:n.145+31_145+32insGA
NM_004670.4:c.145+31_145+32insGA	NP_004661.2:n.145+31_145+32insGA