Canonical Allele Identifier: CA1926073345
Gene: PAPSS2 HGNC NCBI

Linked Data

dbSNP Id: rs1853437460

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87709344_87709347del , CM000672.2:g.87709344_87709347del GRCh38
NC_000010.10:g.89469101_89469104del , CM000672.1:g.89469101_89469104del GRCh37
NC_000010.9:g.89459081_89459084del NCBI36
NG_012150.1:g.54626_54629del

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.145+31_145+34del MANE Select ENSP00000406157.1:n.145+31_145+34del
ENST00000361175.8:c.145+31_145+34del ENSP00000354436.4:n.145+31_145+34del
ENST00000456849.1:c.145+31_145+34del ENSP00000406157.1:n.145+31_145+34del
ENST00000465996.5:n.167+31_167+34del
ENST00000482258.1:n.188+31_188+34del
NM_001015880.1:c.145+31_145+34del NP_001015880.1:n.145+31_145+34del
NM_004670.3:c.145+31_145+34del NP_004661.2:n.145+31_145+34del
NM_001015880.2:c.145+31_145+34del MANE Select NP_001015880.1:n.145+31_145+34del
NM_004670.4:c.145+31_145+34del NP_004661.2:n.145+31_145+34del