Canonical Allele Identifier: CA1813659792

Gene: SLC30A8

Linked Data

• dbSNP Id: rs1823513730

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117173665_117173672dup , CM000670.2:g.117173665_117173672dup	GRCh38
NC_000008.10:g.118185904_118185911dup , CM000670.1:g.118185904_118185911dup	GRCh37
NC_000008.9:g.118255085_118255092dup	NCBI36
NG_016991.1:g.228393_228400dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.*984_*991dup MANE Select	ENSP00000415011.2:n.*984_*991dup
ENST00000427715.2:c.*984_*991dup	ENSP00000407505.2:n.*984_*991dup
ENST00000456015.6:c.2094_2101dup	ENSP00000415011.2:n.2094_2101dup
ENST00000519688.5:c.*984_*991dup	ENSP00000431069.1:n.*984_*991dup
NM_001172811.1:c.*984_*991dup	NP_001166282.1:n.*984_*991dup
NM_001172813.1:c.*984_*991dup	NP_001166284.1:n.*984_*991dup
NM_001172814.1:c.*984_*991dup	NP_001166285.1:n.*984_*991dup
NM_001172815.1:c.*984_*991dup	NP_001166286.1:n.*984_*991dup
NM_173851.2:c.*984_*991dup	NP_776250.2:n.*984_*991dup
XM_011516881.1:c.*984_*991dup	XP_011515183.1:n.*984_*991dup
XM_011516882.1:c.*984_*991dup	XP_011515184.1:n.*984_*991dup
XR_928566.1:n.920-182_920-175dup
XR_928567.1:n.513-182_513-175dup
XR_928568.1:n.718-182_718-175dup
XR_928569.1:n.761-182_761-175dup
XR_928570.1:n.761-182_761-175dup
NM_001172815.2:c.*984_*991dup	NP_001166286.1:n.*984_*991dup
XM_024447083.1:c.*984_*991dup	XP_024302851.1:n.*984_*991dup
XR_001746038.1:n.705-182_705-175dup
XR_928566.2:n.863-182_863-175dup
XR_928567.2:n.476-182_476-175dup
XR_928568.3:n.716-182_716-175dup
XR_928569.2:n.714-182_714-175dup
XR_928570.2:n.714-182_714-175dup
NM_001172811.2:c.*984_*991dup	NP_001166282.1:n.*984_*991dup
NM_001172813.2:c.*984_*991dup	NP_001166284.1:n.*984_*991dup
NM_001172814.2:c.*984_*991dup	NP_001166285.1:n.*984_*991dup
NM_173851.3:c.*984_*991dup MANE Select	NP_776250.2:n.*984_*991dup
NM_001172815.3:c.*984_*991dup	NP_001166286.1:n.*984_*991dup