Canonical Allele Identifier: CA1344395964
Gene: SSUH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733566_8733569delinsTAGG , CM000665.2:g.8733566_8733569delinsTAGG GRCh38
NC_000003.11:g.8775252_8775255delinsTAGG , CM000665.1:g.8775252_8775255delinsTAGG GRCh37
NC_000003.10:g.8750252_8750255delinsTAGG NCBI36
NG_008797.2:g.4757_4760delinsTAGG , LRG_329:g.4757_4760delinsTAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+8890_64+8893delinsCCTA ENSP00000412333.1:n.64+8890_64+8893delinsCCTA
ENST00000478513.1:n.335+8890_335+8893delinsCCTA
XR_940435.1:n.330+8890_330+8893delinsCCTA
XM_017006530.1:c.-283+8890_-283+8893delinsCCTA XP_016862019.1:n.-283+8890_-283+8893delinsCCTA