Canonical Allele Identifier: CA1344396152
Gene: SSUH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733697_8733699delinsTAG , CM000665.2:g.8733697_8733699delinsTAG GRCh38
NC_000003.11:g.8775383_8775385delinsTAG , CM000665.1:g.8775383_8775385delinsTAG GRCh37
NC_000003.10:g.8750383_8750385delinsTAG NCBI36
NG_008797.2:g.4888_4890delinsTAG , LRG_329:g.4888_4890delinsTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+8760_64+8762delinsCTA ENSP00000412333.1:n.64+8760_64+8762delinsCTA
ENST00000478513.1:n.335+8760_335+8762delinsCTA
XR_940435.1:n.330+8760_330+8762delinsCTA
XM_017006530.1:c.-283+8760_-283+8762delinsCTA XP_016862019.1:n.-283+8760_-283+8762delinsCTA