Canonical Allele Identifier: CA1344396217
Gene: SSUH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733745_8733746delinsCT , CM000665.2:g.8733745_8733746delinsCT GRCh38
NC_000003.11:g.8775431_8775432delinsCT , CM000665.1:g.8775431_8775432delinsCT GRCh37
NC_000003.10:g.8750431_8750432delinsCT NCBI36
NG_008797.2:g.4936_4937delinsCT , LRG_329:g.4936_4937delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000435138.5:c.64+8713_64+8714delinsAG ENSP00000412333.1:n.64+8713_64+8714delins...
ENST00000478513.1:n.335+8713_335+8714delinsAG
XR_940435.1:n.330+8713_330+8714delinsAG
XM_017006530.1:c.-283+8713_-283+8714delinsAG XP_016862019.1:n.-283+8713_-283+8714delin...