Canonical Allele Identifier: CA1813659805

Gene: SLC30A8

Linked Data

• dbSNP Id: rs1823516267

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117173693_117173694del , CM000670.2:g.117173693_117173694del	GRCh38
NC_000008.10:g.118185932_118185933del , CM000670.1:g.118185932_118185933del	GRCh37
NC_000008.9:g.118255113_118255114del	NCBI36
NG_016991.1:g.228421_228422del

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.*1012_*1013del MANE Select	ENSP00000415011.2:n.*1012_*1013del
ENST00000427715.2:c.*1012_*1013del	ENSP00000407505.2:n.*1012_*1013del
ENST00000456015.6:c.2122_2123del	ENSP00000415011.2:n.2122_2123del
ENST00000519688.5:c.*1012_*1013del	ENSP00000431069.1:n.*1012_*1013del
NM_001172811.1:c.*1012_*1013del	NP_001166282.1:n.*1012_*1013del
NM_001172813.1:c.*1012_*1013del	NP_001166284.1:n.*1012_*1013del
NM_001172814.1:c.*1012_*1013del	NP_001166285.1:n.*1012_*1013del
NM_001172815.1:c.*1012_*1013del	NP_001166286.1:n.*1012_*1013del
NM_173851.2:c.*1012_*1013del	NP_776250.2:n.*1012_*1013del
XM_011516881.1:c.*1012_*1013del	XP_011515183.1:n.*1012_*1013del
XM_011516882.1:c.*1012_*1013del	XP_011515184.1:n.*1012_*1013del
XR_928566.1:n.920-205_920-204del
XR_928567.1:n.513-205_513-204del
XR_928568.1:n.718-205_718-204del
XR_928569.1:n.761-205_761-204del
XR_928570.1:n.761-205_761-204del
NM_001172815.2:c.*1012_*1013del	NP_001166286.1:n.*1012_*1013del
XM_024447083.1:c.*1012_*1013del	XP_024302851.1:n.*1012_*1013del
XR_001746038.1:n.705-205_705-204del
XR_928566.2:n.863-205_863-204del
XR_928567.2:n.476-205_476-204del
XR_928568.3:n.716-205_716-204del
XR_928569.2:n.714-205_714-204del
XR_928570.2:n.714-205_714-204del
NM_001172811.2:c.*1012_*1013del	NP_001166282.1:n.*1012_*1013del
NM_001172813.2:c.*1012_*1013del	NP_001166284.1:n.*1012_*1013del
NM_001172814.2:c.*1012_*1013del	NP_001166285.1:n.*1012_*1013del
NM_173851.3:c.*1012_*1013del MANE Select	NP_776250.2:n.*1012_*1013del
NM_001172815.3:c.*1012_*1013del	NP_001166286.1:n.*1012_*1013del