Canonical Allele Identifier: CA555411376
Gene: HHIP HGNC NCBI

Linked Data

dbSNP Id: rs1239986460
gnomAD v2: 4-145649929-TG-T
gnomAD v3: 4-144728777-TG-T
gnomAD v4: 4-144728777-TG-T
MyVariant Identifiers: chr4:g.145649930del (hg19) chr4:g.144728778del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144728779del , CM000666.2:g.144728779del GRCh38
NC_000004.11:g.145649931del , CM000666.1:g.145649931del GRCh37
NC_000004.10:g.145869381del NCBI36
NG_011496.1:g.87759del

Transcript Alleles

HGVS Amino-acid change
ENST00000296575.8:c.1761-5962del MANE Select ENSP00000296575.3:n.1761-5962del
ENST00000649263.1:c.328-312800del ENSP00000497507.1:n.328-312800del
ENST00000296575.7:c.1761-5962del ENSP00000296575.3:n.1761-5962del
NM_022475.2:c.1761-5962del NP_071920.1:n.1761-5962del
XM_005263178.3:c.1761-5962del XP_005263235.1:n.1761-5962del
XM_006714288.2:c.1761-5962del XP_006714351.1:n.1761-5962del
XM_005263178.5:c.1761-5962del XP_005263235.1:n.1761-5962del
XM_006714288.4:c.1761-5962del XP_006714351.1:n.1761-5962del
NM_022475.3:c.1761-5962del MANE Select NP_071920.1:n.1761-5962del
Search 100 bp 5'
Search 100 bp 3'