Canonical Allele Identifier: CA1813659410
Gene: SLC30A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117172751T= , CM000670.2:g.117172751T= GRCh38
NC_000008.10:g.118184990T= , CM000670.1:g.118184990T= GRCh37
NC_000008.9:g.118254171T= NCBI36
NG_016991.1:g.227479T=

Transcript Alleles

HGVS Amino-acid change
ENST00000456015.7:c.*70T= MANE Select ENSP00000415011.2:n.*70T=
ENST00000427715.2:c.*70T= ENSP00000407505.2:n.*70T=
ENST00000456015.6:c.1180T= ENSP00000415011.2:n.1180T=
ENST00000519688.5:c.*70T= ENSP00000431069.1:n.*70T=
ENST00000521243.5:c.*70T= ENSP00000428545.1:n.*70T=
NM_001172811.1:c.*70T= NP_001166282.1:n.*70T=
NM_001172813.1:c.*70T= NP_001166284.1:n.*70T=
NM_001172814.1:c.*70T= NP_001166285.1:n.*70T=
NM_001172815.1:c.*70T= NP_001166286.1:n.*70T=
NM_173851.2:c.*70T= NP_776250.2:n.*70T=
XM_011516881.1:c.*70T= XP_011515183.1:n.*70T=
XM_011516882.1:c.*70T= XP_011515184.1:n.*70T=
XR_928569.1:n.890-6A=
XR_928570.1:n.890-6A=
NM_001172815.2:c.*70T= NP_001166286.1:n.*70T=
XM_024447083.1:c.*70T= XP_024302851.1:n.*70T=
XR_928569.2:n.843-6A=
XR_928570.2:n.843-6A=
NM_001172811.2:c.*70T= NP_001166282.1:n.*70T=
NM_001172813.2:c.*70T= NP_001166284.1:n.*70T=
NM_001172814.2:c.*70T= NP_001166285.1:n.*70T=
NM_173851.3:c.*70T= MANE Select NP_776250.2:n.*70T=
NM_001172815.3:c.*70T= NP_001166286.1:n.*70T=