Canonical Allele Identifier: CA2610036381
Gene: PAPSS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87713271_87713272insAATGCAGAC , CM000672.2:g.87713271_87713272insAATGCAGAC GRCh38
NC_000010.10:g.89473028_89473029insAATGCAGAC , CM000672.1:g.89473028_89473029insAATGCAGAC GRCh37
NC_000010.9:g.89463008_89463009insAATGCAGAC NCBI36
NG_012150.1:g.58553_58554insAATGCAGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.342_343insAATGCAGAC MANE Select ENSP00000406157.1:p.Gly114_Leu115insAsnAlaAsp
ENST00000361175.8:c.342_343insAATGCAGAC ENSP00000354436.4:p.Gly114_Leu115insAsnAlaAsp
ENST00000456849.1:c.342_343insAATGCAGAC ENSP00000406157.1:p.Gly114_Leu115insAsnAlaAsp
ENST00000482258.1:n.385_386insAATGCAGAC
NM_001015880.1:c.342_343insAATGCAGAC NP_001015880.1:p.Gly114_Leu115insAsnAlaAsp
NM_004670.3:c.342_343insAATGCAGAC NP_004661.2:p.Gly114_Leu115insAsnAlaAsp
NM_001015880.2:c.342_343insAATGCAGAC MANE Select NP_001015880.1:p.Gly114_Leu115insAsnAlaAsp
NM_004670.4:c.342_343insAATGCAGAC NP_004661.2:p.Gly114_Leu115insAsnAlaAsp