Canonical Allele Identifier: CA1118291147
Gene: SLC30A8 HGNC NCBI

Linked Data

dbSNP Id: rs1823458304

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117172810_117172813dup , CM000670.2:g.117172810_117172813dup GRCh38
NC_000008.10:g.118185049_118185052dup , CM000670.1:g.118185049_118185052dup GRCh37
NC_000008.9:g.118254230_118254233dup NCBI36
NG_016991.1:g.227538_227541dup

Transcript Alleles

HGVS Amino-acid change
ENST00000456015.7:c.*129_*132dup MANE Select ENSP00000415011.2:n.*129_*132dup
ENST00000427715.2:c.*129_*132dup ENSP00000407505.2:n.*129_*132dup
ENST00000456015.6:c.1239_1242dup ENSP00000415011.2:n.1239_1242dup
ENST00000519688.5:c.*129_*132dup ENSP00000431069.1:n.*129_*132dup
NM_001172811.1:c.*129_*132dup NP_001166282.1:n.*129_*132dup
NM_001172813.1:c.*129_*132dup NP_001166284.1:n.*129_*132dup
NM_001172814.1:c.*129_*132dup NP_001166285.1:n.*129_*132dup
NM_001172815.1:c.*129_*132dup NP_001166286.1:n.*129_*132dup
NM_173851.2:c.*129_*132dup NP_776250.2:n.*129_*132dup
XM_011516881.1:c.*129_*132dup XP_011515183.1:n.*129_*132dup
XM_011516882.1:c.*129_*132dup XP_011515184.1:n.*129_*132dup
XR_928569.1:n.890-65_890-62dup
XR_928570.1:n.890-65_890-62dup
NM_001172815.2:c.*129_*132dup NP_001166286.1:n.*129_*132dup
XM_024447083.1:c.*129_*132dup XP_024302851.1:n.*129_*132dup
XR_928569.2:n.843-65_843-62dup
XR_928570.2:n.843-65_843-62dup
NM_001172811.2:c.*129_*132dup NP_001166282.1:n.*129_*132dup
NM_001172813.2:c.*129_*132dup NP_001166284.1:n.*129_*132dup
NM_001172814.2:c.*129_*132dup NP_001166285.1:n.*129_*132dup
NM_173851.3:c.*129_*132dup MANE Select NP_776250.2:n.*129_*132dup
NM_001172815.3:c.*129_*132dup NP_001166286.1:n.*129_*132dup