Canonical Allele Identifier: CA377489586
Gene: PAPSS2 HGNC NCBI

Linked Data

COSMIC: COSM322474

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727433G>A , CM000672.2:g.87727433G>A GRCh38
NC_000010.10:g.89487190G>A , CM000672.1:g.89487190G>A GRCh37
NC_000010.9:g.89477170G>A NCBI36
NG_012150.1:g.72715G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.1030G>A MANE Select ENSP00000406157.1:p.Glu344Lys
ENST00000361175.8:c.1015G>A ENSP00000354436.4:p.Glu339Lys
ENST00000456849.1:c.1030G>A ENSP00000406157.1:p.Glu344Lys
NM_001015880.1:c.1030G>A NP_001015880.1:p.Glu344Lys
NM_004670.3:c.1015G>A NP_004661.2:p.Glu339Lys
NM_001015880.2:c.1030G>A MANE Select NP_001015880.1:p.Glu344Lys
NM_004670.4:c.1015G>A NP_004661.2:p.Glu339Lys