Canonical Allele Identifier: CA1926073307
Gene: PAPSS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87709274_87709275delinsAC , CM000672.2:g.87709274_87709275delinsAC GRCh38
NC_000010.10:g.89469031_89469032delinsAC , CM000672.1:g.89469031_89469032delinsAC GRCh37
NC_000010.9:g.89459011_89459012delinsAC NCBI36
NG_012150.1:g.54556_54557delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.106_107delinsAC MANE Select ENSP00000406157.1:p.Thr36=
ENST00000361175.8:c.106_107delinsAC ENSP00000354436.4:p.Thr36=
ENST00000456849.1:c.106_107delinsAC ENSP00000406157.1:p.Thr36=
ENST00000465996.5:n.128_129delinsAC
ENST00000482258.1:n.149_150delinsAC
NM_001015880.1:c.106_107delinsAC NP_001015880.1:p.Thr36=
NM_004670.3:c.106_107delinsAC NP_004661.2:p.Thr36=
NM_001015880.2:c.106_107delinsAC MANE Select NP_001015880.1:p.Thr36=
NM_004670.4:c.106_107delinsAC NP_004661.2:p.Thr36=
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