Canonical Allele Identifier: CA2515852607
Gene: IP6K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49735259_49735260insCA , CM000665.2:g.49735259_49735260insCA GRCh38
NC_000003.11:g.49772692_49772693insCA , CM000665.1:g.49772692_49772693insCA GRCh37
NC_000003.10:g.49747696_49747697insCA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000321599.9:c.435-2288_435-2287insTG MANE Select ENSP00000323780.4:n.435-2288_435-2287insT...
ENST00000321599.8:c.435-2288_435-2287insTG ENSP00000323780.4:n.435-2288_435-2287insT...
ENST00000395238.5:c.-61-2288_-61-2287insTG ENSP00000378659.1:n.-61-2288_-61-2287insT...
ENST00000460540.1:c.-61-2288_-61-2287insTG ENSP00000420762.1:n.-61-2288_-61-2287insT...
ENST00000468463.5:c.435-2288_435-2287insTG ENSP00000420467.1:n.435-2288_435-2287insT...
ENST00000613416.4:c.435-2288_435-2287insTG ENSP00000482032.1:n.435-2288_435-2287insT...
NM_001006115.2:c.-61-2288_-61-2287insTG NP_001006115.1:n.-61-2288_-61-2287insTG
NM_001242829.1:c.435-2288_435-2287insTG NP_001229758.1:n.435-2288_435-2287insTG
NM_153273.3:c.435-2288_435-2287insTG NP_695005.1:n.435-2288_435-2287insTG
NM_153273.4:c.435-2288_435-2287insTG MANE Select NP_695005.1:n.435-2288_435-2287insTG
NM_001006115.3:c.-61-2288_-61-2287insTG NP_001006115.1:n.-61-2288_-61-2287insTG
NM_001242829.2:c.435-2288_435-2287insTG NP_001229758.1:n.435-2288_435-2287insTG