Canonical Allele Identifier: CA1926063593

Gene: PAPSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727518_87727519delinsTC , CM000672.2:g.87727518_87727519delinsTC	GRCh38
NC_000010.10:g.89487275_89487276delinsTC , CM000672.1:g.89487275_89487276delinsTC	GRCh37
NC_000010.9:g.89477255_89477256delinsTC	NCBI36
NG_012150.1:g.72800_72801delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.1086+29_1086+30delinsTC MANE Select	ENSP00000406157.1:n.1086+29_1086+30delinsTC
ENST00000361175.8:c.1071+29_1071+30delinsTC	ENSP00000354436.4:n.1071+29_1071+30delinsTC
ENST00000456849.1:c.1086+29_1086+30delinsTC	ENSP00000406157.1:n.1086+29_1086+30delinsTC
NM_001015880.1:c.1086+29_1086+30delinsTC	NP_001015880.1:n.1086+29_1086+30delinsTC
NM_004670.3:c.1071+29_1071+30delinsTC	NP_004661.2:n.1071+29_1071+30delinsTC
NM_001015880.2:c.1086+29_1086+30delinsTC MANE Select	NP_001015880.1:n.1086+29_1086+30delinsTC
NM_004670.4:c.1071+29_1071+30delinsTC	NP_004661.2:n.1071+29_1071+30delinsTC