Canonical Allele Identifier: CA1363627653
Gene: IP6K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49735145A= , CM000665.2:g.49735145A= GRCh38
NC_000003.11:g.49772578A= , CM000665.1:g.49772578A= GRCh37
NC_000003.10:g.49747582A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000321599.9:c.435-2173T= MANE Select ENSP00000323780.4:n.435-2173T=
ENST00000321599.8:c.435-2173T= ENSP00000323780.4:n.435-2173T=
ENST00000395238.5:c.-61-2173T= ENSP00000378659.1:n.-61-2173T=
ENST00000460540.1:c.-61-2173T= ENSP00000420762.1:n.-61-2173T=
ENST00000468463.5:c.435-2173T= ENSP00000420467.1:n.435-2173T=
ENST00000613416.4:c.435-2173T= ENSP00000482032.1:n.435-2173T=
NM_001006115.2:c.-61-2173T= NP_001006115.1:n.-61-2173T=
NM_001242829.1:c.435-2173T= NP_001229758.1:n.435-2173T=
NM_153273.3:c.435-2173T= NP_695005.1:n.435-2173T=
NM_153273.4:c.435-2173T= MANE Select NP_695005.1:n.435-2173T=
NM_001006115.3:c.-61-2173T= NP_001006115.1:n.-61-2173T=
NM_001242829.2:c.435-2173T= NP_001229758.1:n.435-2173T=