Canonical Allele Identifier: CA1813625412

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117142787_117142789delinsCTA , CM000670.2:g.117142787_117142789delinsCTA	GRCh38
NC_000008.10:g.118155026_118155028delinsCTA , CM000670.1:g.118155026_118155028delinsCTA	GRCh37
NC_000008.9:g.118224207_118224209delinsCTA	NCBI36
NG_016991.1:g.197515_197517delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.72-4167_72-4165delinsCTA MANE Select	ENSP00000415011.2:n.72-4167_72-4165delinsCTA
ENST00000427715.2:c.-106-4032_-106-4030delinsCTA	ENSP00000407505.2:n.-106-4032_-106-4030delinsCTA
ENST00000456015.6:c.72-4167_72-4165delinsCTA	ENSP00000415011.2:n.72-4167_72-4165delinsCTA
ENST00000518396.5:c.-106-4032_-106-4030delinsCTA	ENSP00000485167.1:n.-106-4032_-106-4030delinsCTA
ENST00000518521.5:c.-76-4167_-76-4165delinsCTA	ENSP00000485566.1:n.-76-4167_-76-4165delinsCTA
ENST00000519688.5:c.-106-4032_-106-4030delinsCTA	ENSP00000431069.1:n.-106-4032_-106-4030delinsCTA
ENST00000520469.1:n.326-4167_326-4165delinsCTA
ENST00000521035.5:n.462-4032_462-4030delinsCTA
ENST00000521243.5:c.-106-4032_-106-4030delinsCTA	ENSP00000428545.1:n.-106-4032_-106-4030delinsCTA
ENST00000524274.5:c.-106-4032_-106-4030delinsCTA	ENSP00000427760.1:n.-106-4032_-106-4030delinsCTA
NM_001172811.1:c.-106-4032_-106-4030delinsCTA	NP_001166282.1:n.-106-4032_-106-4030delinsCTA
NM_001172813.1:c.-106-4032_-106-4030delinsCTA	NP_001166284.1:n.-106-4032_-106-4030delinsCTA
NM_001172814.1:c.-106-4032_-106-4030delinsCTA	NP_001166285.1:n.-106-4032_-106-4030delinsCTA
NM_001172815.1:c.-106-4032_-106-4030delinsCTA	NP_001166286.1:n.-106-4032_-106-4030delinsCTA
NM_173851.2:c.72-4167_72-4165delinsCTA	NP_776250.2:n.72-4167_72-4165delinsCTA
XM_011516881.1:c.72-4167_72-4165delinsCTA	XP_011515183.1:n.72-4167_72-4165delinsCTA
XR_928569.1:n.1020+29826_1020+29828delinsTAG
XR_928570.1:n.1021-25003_1021-25001delinsTAG
NM_001172815.2:c.-106-4032_-106-4030delinsCTA	NP_001166286.1:n.-106-4032_-106-4030delinsCTA
XM_024447083.1:c.-106-4032_-106-4030delinsCTA	XP_024302851.1:n.-106-4032_-106-4030delinsCTA
XR_928569.2:n.973+29826_973+29828delinsTAG
XR_928570.2:n.974-25003_974-25001delinsTAG
NM_001172811.2:c.-106-4032_-106-4030delinsCTA	NP_001166282.1:n.-106-4032_-106-4030delinsCTA
NM_001172813.2:c.-106-4032_-106-4030delinsCTA	NP_001166284.1:n.-106-4032_-106-4030delinsCTA
NM_001172814.2:c.-106-4032_-106-4030delinsCTA	NP_001166285.1:n.-106-4032_-106-4030delinsCTA
NM_173851.3:c.72-4167_72-4165delinsCTA MANE Select	NP_776250.2:n.72-4167_72-4165delinsCTA
NM_001172815.3:c.-106-4032_-106-4030delinsCTA	NP_001166286.1:n.-106-4032_-106-4030delinsCTA