Canonical Allele Identifier: CA1344395798
Gene: SSUH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733473_8733474delinsGT , CM000665.2:g.8733473_8733474delinsGT GRCh38
NC_000003.11:g.8775159_8775160delinsGT , CM000665.1:g.8775159_8775160delinsGT GRCh37
NC_000003.10:g.8750159_8750160delinsGT NCBI36
NG_008797.2:g.4664_4665delinsGT , LRG_329:g.4664_4665delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+8985_64+8986delinsAC ENSP00000412333.1:n.64+8985_64+8986delinsAC
ENST00000478513.1:n.335+8985_335+8986delinsAC
XR_940435.1:n.330+8985_330+8986delinsAC
XM_017006530.1:c.-283+8985_-283+8986delinsAC XP_016862019.1:n.-283+8985_-283+8986delinsAC