Canonical Allele Identifier: CA653008293

Gene: SLC30A8

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117172802_117172803insT , CM000670.2:g.117172802_117172803insT	GRCh38
NC_000008.10:g.118185041_118185042insT , CM000670.1:g.118185041_118185042insT	GRCh37
NC_000008.9:g.118254222_118254223insT	NCBI36
NG_016991.1:g.227530_227531insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.*121_*122insT MANE Select	ENSP00000415011.2:n.*121_*122insT
ENST00000427715.2:c.*121_*122insT	ENSP00000407505.2:n.*121_*122insT
ENST00000456015.6:c.1231_1232insT	ENSP00000415011.2:n.1231_1232insT
ENST00000519688.5:c.*121_*122insT	ENSP00000431069.1:n.*121_*122insT
NM_001172811.1:c.*121_*122insT	NP_001166282.1:n.*121_*122insT
NM_001172813.1:c.*121_*122insT	NP_001166284.1:n.*121_*122insT
NM_001172814.1:c.*121_*122insT	NP_001166285.1:n.*121_*122insT
NM_001172815.1:c.*121_*122insT	NP_001166286.1:n.*121_*122insT
NM_173851.2:c.*121_*122insT	NP_776250.2:n.*121_*122insT
XM_011516881.1:c.*121_*122insT	XP_011515183.1:n.*121_*122insT
XM_011516882.1:c.*121_*122insT	XP_011515184.1:n.*121_*122insT
XR_928569.1:n.890-58_890-57insA
XR_928570.1:n.890-58_890-57insA
NM_001172815.2:c.*121_*122insT	NP_001166286.1:n.*121_*122insT
XM_024447083.1:c.*121_*122insT	XP_024302851.1:n.*121_*122insT
XR_928569.2:n.843-58_843-57insA
XR_928570.2:n.843-58_843-57insA
NM_001172811.2:c.*121_*122insT	NP_001166282.1:n.*121_*122insT
NM_001172813.2:c.*121_*122insT	NP_001166284.1:n.*121_*122insT
NM_001172814.2:c.*121_*122insT	NP_001166285.1:n.*121_*122insT
NM_173851.3:c.*121_*122insT MANE Select	NP_776250.2:n.*121_*122insT
NM_001172815.3:c.*121_*122insT	NP_001166286.1:n.*121_*122insT