Canonical Allele Identifier: CA1118291339

Gene: SLC30A8

Linked Data

• dbSNP Id: rs1823496590
• gnomAD v3: 8-117173432-C-CA
• gnomAD v4: 8-117173432-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117173437dup , CM000670.2:g.117173437dup	GRCh38
NC_000008.10:g.118185676dup , CM000670.1:g.118185676dup	GRCh37
NC_000008.9:g.118254857dup	NCBI36
NG_016991.1:g.228165dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.*756dup MANE Select	ENSP00000415011.2:n.*756dup
ENST00000427715.2:c.*756dup	ENSP00000407505.2:n.*756dup
ENST00000456015.6:c.1866dup	ENSP00000415011.2:n.1866dup
ENST00000519688.5:c.*756dup	ENSP00000431069.1:n.*756dup
NM_001172811.1:c.*756dup	NP_001166282.1:n.*756dup
NM_001172813.1:c.*756dup	NP_001166284.1:n.*756dup
NM_001172814.1:c.*756dup	NP_001166285.1:n.*756dup
NM_001172815.1:c.*756dup	NP_001166286.1:n.*756dup
NM_173851.2:c.*756dup	NP_776250.2:n.*756dup
XM_011516881.1:c.*756dup	XP_011515183.1:n.*756dup
XM_011516882.1:c.*756dup	XP_011515184.1:n.*756dup
XR_928566.1:n.975dup
XR_928567.1:n.568dup
XR_928568.1:n.773dup
XR_928569.1:n.816dup
XR_928570.1:n.816dup
NM_001172815.2:c.*756dup	NP_001166286.1:n.*756dup
XM_024447083.1:c.*756dup	XP_024302851.1:n.*756dup
XR_001746038.1:n.760dup
XR_928566.2:n.918dup
XR_928567.2:n.531dup
XR_928568.3:n.771dup
XR_928569.2:n.769dup
XR_928570.2:n.769dup
NM_001172811.2:c.*756dup	NP_001166282.1:n.*756dup
NM_001172813.2:c.*756dup	NP_001166284.1:n.*756dup
NM_001172814.2:c.*756dup	NP_001166285.1:n.*756dup
NM_173851.3:c.*756dup MANE Select	NP_776250.2:n.*756dup
NM_001172815.3:c.*756dup	NP_001166286.1:n.*756dup