Canonical Allele Identifier: CA1813625418

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117142795_117142797delinsCCT , CM000670.2:g.117142795_117142797delinsCCT	GRCh38
NC_000008.10:g.118155034_118155036delinsCCT , CM000670.1:g.118155034_118155036delinsCCT	GRCh37
NC_000008.9:g.118224215_118224217delinsCCT	NCBI36
NG_016991.1:g.197523_197525delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.72-4159_72-4157delinsCCT MANE Select	ENSP00000415011.2:n.72-4159_72-4157delinsCCT
ENST00000427715.2:c.-106-4024_-106-4022delinsCCT	ENSP00000407505.2:n.-106-4024_-106-4022delinsCCT
ENST00000456015.6:c.72-4159_72-4157delinsCCT	ENSP00000415011.2:n.72-4159_72-4157delinsCCT
ENST00000518396.5:c.-106-4024_-106-4022delinsCCT	ENSP00000485167.1:n.-106-4024_-106-4022delinsCCT
ENST00000518521.5:c.-76-4159_-76-4157delinsCCT	ENSP00000485566.1:n.-76-4159_-76-4157delinsCCT
ENST00000519688.5:c.-106-4024_-106-4022delinsCCT	ENSP00000431069.1:n.-106-4024_-106-4022delinsCCT
ENST00000520469.1:n.326-4159_326-4157delinsCCT
ENST00000521035.5:n.462-4024_462-4022delinsCCT
ENST00000521243.5:c.-106-4024_-106-4022delinsCCT	ENSP00000428545.1:n.-106-4024_-106-4022delinsCCT
ENST00000524274.5:c.-106-4024_-106-4022delinsCCT	ENSP00000427760.1:n.-106-4024_-106-4022delinsCCT
NM_001172811.1:c.-106-4024_-106-4022delinsCCT	NP_001166282.1:n.-106-4024_-106-4022delinsCCT
NM_001172813.1:c.-106-4024_-106-4022delinsCCT	NP_001166284.1:n.-106-4024_-106-4022delinsCCT
NM_001172814.1:c.-106-4024_-106-4022delinsCCT	NP_001166285.1:n.-106-4024_-106-4022delinsCCT
NM_001172815.1:c.-106-4024_-106-4022delinsCCT	NP_001166286.1:n.-106-4024_-106-4022delinsCCT
NM_173851.2:c.72-4159_72-4157delinsCCT	NP_776250.2:n.72-4159_72-4157delinsCCT
XM_011516881.1:c.72-4159_72-4157delinsCCT	XP_011515183.1:n.72-4159_72-4157delinsCCT
XR_928569.1:n.1020+29818_1020+29820delinsAGG
XR_928570.1:n.1021-25011_1021-25009delinsAGG
NM_001172815.2:c.-106-4024_-106-4022delinsCCT	NP_001166286.1:n.-106-4024_-106-4022delinsCCT
XM_024447083.1:c.-106-4024_-106-4022delinsCCT	XP_024302851.1:n.-106-4024_-106-4022delinsCCT
XR_928569.2:n.973+29818_973+29820delinsAGG
XR_928570.2:n.974-25011_974-25009delinsAGG
NM_001172811.2:c.-106-4024_-106-4022delinsCCT	NP_001166282.1:n.-106-4024_-106-4022delinsCCT
NM_001172813.2:c.-106-4024_-106-4022delinsCCT	NP_001166284.1:n.-106-4024_-106-4022delinsCCT
NM_001172814.2:c.-106-4024_-106-4022delinsCCT	NP_001166285.1:n.-106-4024_-106-4022delinsCCT
NM_173851.3:c.72-4159_72-4157delinsCCT MANE Select	NP_776250.2:n.72-4159_72-4157delinsCCT
NM_001172815.3:c.-106-4024_-106-4022delinsCCT	NP_001166286.1:n.-106-4024_-106-4022delinsCCT