Canonical Allele Identifier: CA2517684757
Gene: PAPSS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727105_87727111del , CM000672.2:g.87727105_87727111del GRCh38
NC_000010.10:g.89486862_89486868del , CM000672.1:g.89486862_89486868del GRCh37
NC_000010.9:g.89476842_89476848del NCBI36
NG_012150.1:g.72387_72393del

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.881-179_881-173del MANE Select ENSP00000406157.1:n.881-179_881-173del
ENST00000361175.8:c.866-179_866-173del ENSP00000354436.4:n.866-179_866-173del
ENST00000456849.1:c.881-179_881-173del ENSP00000406157.1:n.881-179_881-173del
NM_001015880.1:c.881-179_881-173del NP_001015880.1:n.881-179_881-173del
NM_004670.3:c.866-179_866-173del NP_004661.2:n.866-179_866-173del
NM_001015880.2:c.881-179_881-173del MANE Select NP_001015880.1:n.881-179_881-173del
NM_004670.4:c.866-179_866-173del NP_004661.2:n.866-179_866-173del