Canonical Allele Identifier: CA824098881

Gene: IP6K3

Linked Data

• dbSNP Id: rs556727474
• gnomAD v3: 6-33738662-G-T
• gnomAD v4: 6-33738662-G-T
• MyVariant Identifiers: chr6:g.33706439G>T (hg19) ; chr6:g.33738662G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33738662G>T , CM000668.2:g.33738662G>T	GRCh38
NC_000006.11:g.33706439G>T , CM000668.1:g.33706439G>T	GRCh37
NC_000006.10:g.33814417G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293756.5:c.-179-3007C>A MANE Select	ENSP00000293756.4:n.-179-3007C>A
ENST00000293756.4:c.-179-3007C>A	ENSP00000293756.4:n.-179-3007C>A
ENST00000451316.6:c.-180+471C>A	ENSP00000398861.1:n.-180+471C>A
ENST00000634274.1:c.-179-3007C>A	ENSP00000489479.1:n.-179-3007C>A
NM_001142883.1:c.-180+471C>A	NP_001136355.1:n.-180+471C>A
NM_054111.4:c.-179-3007C>A	NP_473452.2:n.-179-3007C>A
XM_005248842.2:c.-179-3007C>A	XP_005248899.1:n.-179-3007C>A
XM_011514295.1:c.-179-3007C>A	XP_011512597.1:n.-179-3007C>A
XM_005248842.3:c.-179-3007C>A	XP_005248899.1:n.-179-3007C>A
XM_005248843.4:c.-768-3007C>A	XP_005248900.1:n.-768-3007C>A
XM_011514295.3:c.-179-3007C>A	XP_011512597.1:n.-179-3007C>A
XM_024446323.1:c.-180+471C>A	XP_024302091.1:n.-180+471C>A
XM_024446324.1:c.-180+471C>A	XP_024302092.1:n.-180+471C>A
XM_024446325.1:c.-179-3007C>A	XP_024302093.1:n.-179-3007C>A
XM_024446326.1:c.-769+471C>A	XP_024302094.1:n.-769+471C>A
XM_024446327.1:c.-768-3007C>A	XP_024302095.1:n.-768-3007C>A
NM_054111.5:c.-179-3007C>A MANE Select	NP_473452.2:n.-179-3007C>A
NM_001142883.2:c.-180+471C>A	NP_001136355.1:n.-180+471C>A