Canonical Allele Identifier: CA1363626090
Gene: IP6K1 HGNC NCBI

Linked Data

dbSNP Id: rs2080561417

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49731523_49731530del , CM000665.2:g.49731523_49731530del GRCh38
NC_000003.11:g.49768956_49768963del , CM000665.1:g.49768956_49768963del GRCh37
NC_000003.10:g.49743960_49743967del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000321599.9:c.616+1261_616+1268del MANE Select ENSP00000323780.4:n.616+1261_616+1268del
ENST00000321599.8:c.616+1261_616+1268del ENSP00000323780.4:n.616+1261_616+1268del
ENST00000395238.5:c.121+1261_121+1268del ENSP00000378659.1:n.121+1261_121+1268del
ENST00000460540.1:c.121+1261_121+1268del ENSP00000420762.1:n.121+1261_121+1268del
ENST00000468463.5:c.616+1261_616+1268del ENSP00000420467.1:n.616+1261_616+1268del
ENST00000613416.4:c.616+1261_616+1268del ENSP00000482032.1:n.616+1261_616+1268del
NM_001006115.2:c.121+1261_121+1268del NP_001006115.1:n.121+1261_121+1268del
NM_001242829.1:c.616+1261_616+1268del NP_001229758.1:n.616+1261_616+1268del
NM_153273.3:c.616+1261_616+1268del NP_695005.1:n.616+1261_616+1268del
NM_153273.4:c.616+1261_616+1268del MANE Select NP_695005.1:n.616+1261_616+1268del
NM_001006115.3:c.121+1261_121+1268del NP_001006115.1:n.121+1261_121+1268del
NM_001242829.2:c.616+1261_616+1268del NP_001229758.1:n.616+1261_616+1268del