Canonical Allele Identifier: CA1813625332

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117142613_117142639delinsTCTTTGGGCATTTGCTCCAGCAATGCC , CM000670.2:g.117142613_117142639delinsTCTTTGGGCATTTGCTCCAGCAATGCC	GRCh38
NC_000008.10:g.118154852_118154878delinsTCTTTGGGCATTTGCTCCAGCAATGCC , CM000670.1:g.118154852_118154878delinsTCTTTGGGCATTTGCTCCAGCAATGCC	GRCh37
NC_000008.9:g.118224033_118224059delinsTCTTTGGGCATTTGCTCCAGCAATGCC	NCBI36
NG_016991.1:g.197341_197367delinsTCTTTGGGCATTTGCTCCAGCAATGCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.72-4341_72-4315delinsTCTTTGGGCATTTGCTCCAGCAATGCC MANE Select	ENSP00000415011.2:n.72-4341_72-4315delinsTCTTTGGGCATTTGCTCCAG...
ENST00000427715.2:c.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCAGCAATGCC	ENSP00000407505.2:n.-106-4206_-106-4180delinsTCTTTGGGCATTTGCT...
ENST00000456015.6:c.72-4341_72-4315delinsTCTTTGGGCATTTGCTCCAGCAATGCC	ENSP00000415011.2:n.72-4341_72-4315delinsTCTTTGGGCATTTGCTCCAG...
ENST00000518396.5:c.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCAGCAATGCC	ENSP00000485167.1:n.-106-4206_-106-4180delinsTCTTTGGGCATTTGCT...
ENST00000518521.5:c.-76-4341_-76-4315delinsTCTTTGGGCATTTGCTCCAGCAATGCC	ENSP00000485566.1:n.-76-4341_-76-4315delinsTCTTTGGGCATTTGCTCC...
ENST00000519688.5:c.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCAGCAATGCC	ENSP00000431069.1:n.-106-4206_-106-4180delinsTCTTTGGGCATTTGCT...
ENST00000520469.1:n.326-4341_326-4315delinsTCTTTGGGCATTTGCTCCAGCAATGCC
ENST00000521035.5:n.462-4206_462-4180delinsTCTTTGGGCATTTGCTCCAGCAATGCC
ENST00000521243.5:c.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCAGCAATGCC	ENSP00000428545.1:n.-106-4206_-106-4180delinsTCTTTGGGCATTTGCT...
ENST00000524274.5:c.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCAGCAATGCC	ENSP00000427760.1:n.-106-4206_-106-4180delinsTCTTTGGGCATTTGCT...
NM_001172811.1:c.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCAGCAATGCC	NP_001166282.1:n.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCA...
NM_001172813.1:c.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCAGCAATGCC	NP_001166284.1:n.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCA...
NM_001172814.1:c.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCAGCAATGCC	NP_001166285.1:n.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCA...
NM_001172815.1:c.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCAGCAATGCC	NP_001166286.1:n.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCA...
NM_173851.2:c.72-4341_72-4315delinsTCTTTGGGCATTTGCTCCAGCAATGCC	NP_776250.2:n.72-4341_72-4315delinsTCTTTGGGCATTTGCTCCAGCAATGC...
XM_011516881.1:c.72-4341_72-4315delinsTCTTTGGGCATTTGCTCCAGCAATGCC	XP_011515183.1:n.72-4341_72-4315delinsTCTTTGGGCATTTGCTCCAGCAA...
XR_928569.1:n.1020+29976_1020+30002delinsGGCATTGCTGGAGCAAATGCCCAAAGA
XR_928570.1:n.1021-24853_1021-24827delinsGGCATTGCTGGAGCAAATGCCCAAAGA
NM_001172815.2:c.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCAGCAATGCC	NP_001166286.1:n.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCA...
XM_024447083.1:c.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCAGCAATGCC	XP_024302851.1:n.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCA...
XR_928569.2:n.973+29976_973+30002delinsGGCATTGCTGGAGCAAATGCCCAAAGA
XR_928570.2:n.974-24853_974-24827delinsGGCATTGCTGGAGCAAATGCCCAAAGA
NM_001172811.2:c.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCAGCAATGCC	NP_001166282.1:n.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCA...
NM_001172813.2:c.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCAGCAATGCC	NP_001166284.1:n.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCA...
NM_001172814.2:c.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCAGCAATGCC	NP_001166285.1:n.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCA...
NM_173851.3:c.72-4341_72-4315delinsTCTTTGGGCATTTGCTCCAGCAATGCC MANE Select	NP_776250.2:n.72-4341_72-4315delinsTCTTTGGGCATTTGCTCCAGCAATGC...
NM_001172815.3:c.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCAGCAATGCC	NP_001166286.1:n.-106-4206_-106-4180delinsTCTTTGGGCATTTGCTCCA...