Canonical Allele Identifier: CA377489592

Gene: PAPSS2

Linked Data

• MyVariant Identifiers: chr10:g.89487192G>C (hg19) ; chr10:g.87727435G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727435G>C , CM000672.2:g.87727435G>C	GRCh38
NC_000010.10:g.89487192G>C , CM000672.1:g.89487192G>C	GRCh37
NC_000010.9:g.89477172G>C	NCBI36
NG_012150.1:g.72717G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.1032G>C MANE Select	ENSP00000406157.1:p.Glu344Asp
ENST00000361175.8:c.1017G>C	ENSP00000354436.4:p.Glu339Asp
ENST00000456849.1:c.1032G>C	ENSP00000406157.1:p.Glu344Asp
NM_001015880.1:c.1032G>C	NP_001015880.1:p.Glu344Asp
NM_004670.3:c.1017G>C	NP_004661.2:p.Glu339Asp
NM_001015880.2:c.1032G>C MANE Select	NP_001015880.1:p.Glu344Asp
NM_004670.4:c.1017G>C	NP_004661.2:p.Glu339Asp