Canonical Allele Identifier: CA4268723
Gene: PSPH HGNC NCBI

Linked Data

ClinVar Variation Id: 403351
dbSNP Id: rs139106189

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.56019600del , CM000669.2:g.56019600del GRCh38
NC_000007.13:g.56087293del , CM000669.1:g.56087293del GRCh37
NC_000007.12:g.56054787del NCBI36
NG_011473.1:g.36977del

Transcript Alleles

HGVS Amino-acid Change
ENST00000275605.8:c.275+1del
ENST00000275605.7:c.275+1del
ENST00000395471.7:c.275+1del
ENST00000421626.5:c.275+1del
ENST00000427797.5:c.*76+1del
ENST00000437355.6:c.275+1del
ENST00000459834.5:n.212-4428del
NM_004577.3:c.275+1del
XM_005271773.1:c.275+1del
XM_005271774.1:c.275+1del
XM_005271775.1:c.275+1del
XM_005271776.1:c.275+1del
XM_006715760.1:c.275+1del
XM_006715761.1:c.140+1474del XP_006715824.1:n.140+1474del
XM_011515459.1:c.275+1del
XM_011515460.1:c.275+1del
XM_011515461.1:c.275+1del
XM_011515462.1:c.275+1del
XM_005271773.2:c.275+1del
XM_005271774.2:c.275+1del
XM_005271775.2:c.275+1del
XM_005271776.2:c.275+1del
XM_006715760.2:c.275+1del
XM_006715761.2:c.140+1474del XP_006715824.1:n.140+1474del
XM_011515461.2:c.275+1del
XM_017012466.2:c.275+1del
XM_017012467.2:c.275+1del
XM_017012468.2:c.140+1474del XP_016867957.1:n.140+1474del
XM_017012469.2:c.140+1474del XP_016867958.1:n.140+1474del
XR_002956470.1:n.1072+1del
NM_004577.4:c.275+1del
NM_001370503.1:c.275+1del
NM_001370504.1:c.275+1del
NM_001370505.1:c.275+1del
NM_001370506.1:c.275+1del
NM_001370507.1:c.275+1del
NM_001370508.1:c.275+1del
NM_001370509.1:c.275+1del
NM_001370510.1:c.275+1del
NM_001370511.1:c.275+1del
NM_001370512.1:c.275+1del
NM_001370513.1:c.275+1del
NM_001370514.1:c.275+1del
NM_001370515.1:c.275+1del
NM_001370516.1:c.275+1del
NM_001370517.1:c.275+1del
NM_001370518.1:c.275+1del
NM_001370519.1:c.275+1del
NM_001370520.1:c.275+1del
NM_001370521.1:c.275+1del
NM_001370522.1:c.275+1del