Canonical Allele Identifier: CA1344395707
Gene: SSUH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733407_8733408delinsTG , CM000665.2:g.8733407_8733408delinsTG GRCh38
NC_000003.11:g.8775093_8775094delinsTG , CM000665.1:g.8775093_8775094delinsTG GRCh37
NC_000003.10:g.8750093_8750094delinsTG NCBI36
NG_008797.2:g.4598_4599delinsTG , LRG_329:g.4598_4599delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+9051_64+9052delinsCA ENSP00000412333.1:n.64+9051_64+9052delinsCA
ENST00000478513.1:n.335+9051_335+9052delinsCA
XR_940435.1:n.330+9051_330+9052delinsCA
XM_017006530.1:c.-283+9051_-283+9052delinsCA XP_016862019.1:n.-283+9051_-283+9052delinsCA