Canonical Allele Identifier: CA1926080783
Gene: PAPSS2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727360_87727361delinsCA , CM000672.2:g.87727360_87727361delinsCA GRCh38
NC_000010.10:g.89487117_89487118delinsCA , CM000672.1:g.89487117_89487118delinsCA GRCh37
NC_000010.9:g.89477097_89477098delinsCA NCBI36
NG_012150.1:g.72642_72643delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.957_958delinsCA MANE Select ENSP00000406157.1:p.Ser319=
ENST00000361175.8:c.942_943delinsCA ENSP00000354436.4:p.Ser314=
ENST00000456849.1:c.957_958delinsCA ENSP00000406157.1:p.Ser319=
NM_001015880.1:c.957_958delinsCA NP_001015880.1:p.Ser319=
NM_004670.3:c.942_943delinsCA NP_004661.2:p.Ser314=
NM_001015880.2:c.957_958delinsCA MANE Select NP_001015880.1:p.Ser319=
NM_004670.4:c.942_943delinsCA NP_004661.2:p.Ser314=
Search 100 bp 5'
Search 100 bp 3'