Canonical Allele Identifier: CA2610034524
Gene: PAPSS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87709345_87709346insTACA , CM000672.2:g.87709345_87709346insTACA GRCh38
NC_000010.10:g.89469102_89469103insTACA , CM000672.1:g.89469102_89469103insTACA GRCh37
NC_000010.9:g.89459082_89459083insTACA NCBI36
NG_012150.1:g.54627_54628insTACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.145+32_145+33insTACA MANE Select ENSP00000406157.1:n.145+32_145+33insTACA
ENST00000361175.8:c.145+32_145+33insTACA ENSP00000354436.4:n.145+32_145+33insTACA
ENST00000456849.1:c.145+32_145+33insTACA ENSP00000406157.1:n.145+32_145+33insTACA
ENST00000465996.5:n.167+32_167+33insTACA
ENST00000482258.1:n.188+32_188+33insTACA
NM_001015880.1:c.145+32_145+33insTACA NP_001015880.1:n.145+32_145+33insTACA
NM_004670.3:c.145+32_145+33insTACA NP_004661.2:n.145+32_145+33insTACA
NM_001015880.2:c.145+32_145+33insTACA MANE Select NP_001015880.1:n.145+32_145+33insTACA
NM_004670.4:c.145+32_145+33insTACA NP_004661.2:n.145+32_145+33insTACA