Canonical Allele Identifier: CA846168925

Gene: SLC30A8

Linked Data

• dbSNP Id: rs1340343660
• gnomAD v3: 8-117173495-GA-G
• gnomAD v4: 8-117173495-GA-G
• MyVariant Identifiers: chr8:g.118185735del (hg19) ; chr8:g.117173496del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117173497del , CM000670.2:g.117173497del	GRCh38
NC_000008.10:g.118185736del , CM000670.1:g.118185736del	GRCh37
NC_000008.9:g.118254917del	NCBI36
NG_016991.1:g.228225del

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.*816del MANE Select	ENSP00000415011.2:n.*816del
ENST00000427715.2:c.*816del	ENSP00000407505.2:n.*816del
ENST00000456015.6:c.1926del	ENSP00000415011.2:n.1926del
ENST00000519688.5:c.*816del	ENSP00000431069.1:n.*816del
NM_001172811.1:c.*816del	NP_001166282.1:n.*816del
NM_001172813.1:c.*816del	NP_001166284.1:n.*816del
NM_001172814.1:c.*816del	NP_001166285.1:n.*816del
NM_001172815.1:c.*816del	NP_001166286.1:n.*816del
NM_173851.2:c.*816del	NP_776250.2:n.*816del
XM_011516881.1:c.*816del	XP_011515183.1:n.*816del
XM_011516882.1:c.*816del	XP_011515184.1:n.*816del
XR_928566.1:n.920-8del
XR_928567.1:n.513-8del
XR_928568.1:n.718-8del
XR_928569.1:n.761-8del
XR_928570.1:n.761-8del
NM_001172815.2:c.*816del	NP_001166286.1:n.*816del
XM_024447083.1:c.*816del	XP_024302851.1:n.*816del
XR_001746038.1:n.705-8del
XR_928566.2:n.863-8del
XR_928567.2:n.476-8del
XR_928568.3:n.716-8del
XR_928569.2:n.714-8del
XR_928570.2:n.714-8del
NM_001172811.2:c.*816del	NP_001166282.1:n.*816del
NM_001172813.2:c.*816del	NP_001166284.1:n.*816del
NM_001172814.2:c.*816del	NP_001166285.1:n.*816del
NM_173851.3:c.*816del MANE Select	NP_776250.2:n.*816del
NM_001172815.3:c.*816del	NP_001166286.1:n.*816del