Canonical Allele Identifier: CA1926063576
Gene: PAPSS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727476_87727477delinsAC , CM000672.2:g.87727476_87727477delinsAC GRCh38
NC_000010.10:g.89487233_89487234delinsAC , CM000672.1:g.89487233_89487234delinsAC GRCh37
NC_000010.9:g.89477213_89477214delinsAC NCBI36
NG_012150.1:g.72758_72759delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.1073_1074delinsAC MANE Select ENSP00000406157.1:p.His358=
ENST00000361175.8:c.1058_1059delinsAC ENSP00000354436.4:p.His353=
ENST00000456849.1:c.1073_1074delinsAC ENSP00000406157.1:p.His358=
NM_001015880.1:c.1073_1074delinsAC NP_001015880.1:p.His358=
NM_004670.3:c.1058_1059delinsAC NP_004661.2:p.His353=
NM_001015880.2:c.1073_1074delinsAC MANE Select NP_001015880.1:p.His358=
NM_004670.4:c.1058_1059delinsAC NP_004661.2:p.His353=