Canonical Allele Identifier: CA907851165

Gene: IP6K1

Linked Data

• dbSNP Id: rs1323044598
• gnomAD v3: 3-49735056-A-T
• gnomAD v4: 3-49735056-A-T
• MyVariant Identifiers: chr3:g.49772489A>T (hg19) ; chr3:g.49735056A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49735056A>T , CM000665.2:g.49735056A>T	GRCh38
NC_000003.11:g.49772489A>T , CM000665.1:g.49772489A>T	GRCh37
NC_000003.10:g.49747493A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321599.9:c.435-2084T>A MANE Select	ENSP00000323780.4:n.435-2084T>A
ENST00000321599.8:c.435-2084T>A	ENSP00000323780.4:n.435-2084T>A
ENST00000395238.5:c.-61-2084T>A	ENSP00000378659.1:n.-61-2084T>A
ENST00000460540.1:c.-61-2084T>A	ENSP00000420762.1:n.-61-2084T>A
ENST00000468463.5:c.435-2084T>A	ENSP00000420467.1:n.435-2084T>A
ENST00000613416.4:c.435-2084T>A	ENSP00000482032.1:n.435-2084T>A
NM_001006115.2:c.-61-2084T>A	NP_001006115.1:n.-61-2084T>A
NM_001242829.1:c.435-2084T>A	NP_001229758.1:n.435-2084T>A
NM_153273.3:c.435-2084T>A	NP_695005.1:n.435-2084T>A
NM_153273.4:c.435-2084T>A MANE Select	NP_695005.1:n.435-2084T>A
NM_001006115.3:c.-61-2084T>A	NP_001006115.1:n.-61-2084T>A
NM_001242829.2:c.435-2084T>A	NP_001229758.1:n.435-2084T>A