Canonical Allele Identifier: CA1813629790
Gene: SLC30A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117152998T= , CM000670.2:g.117152998T= GRCh38
NC_000008.10:g.118165237T= , CM000670.1:g.118165237T= GRCh37
NC_000008.9:g.118234418T= NCBI36
NG_016991.1:g.207726T=

Transcript Alleles

HGVS Amino-acid change
ENST00000456015.7:c.326T= MANE Select ENSP00000415011.2:p.Ile109=
ENST00000427715.2:c.179T= ENSP00000407505.2:p.Ile60=
ENST00000456015.6:c.326T= ENSP00000415011.2:p.Ile109=
ENST00000519688.5:c.179T= ENSP00000431069.1:p.Ile60=
ENST00000521243.5:c.179T= ENSP00000428545.1:p.Ile60=
ENST00000524274.5:c.179T= ENSP00000427760.1:p.Ile60=
NM_001172811.1:c.179T= NP_001166282.1:p.Ile60=
NM_001172813.1:c.179T= NP_001166284.1:p.Ile60=
NM_001172814.1:c.179T= NP_001166285.1:p.Ile60=
NM_001172815.1:c.179T= NP_001166286.1:p.Ile60=
NM_173851.2:c.326T= NP_776250.2:p.Ile109=
XM_011516881.1:c.326T= XP_011515183.1:p.Ile109=
XM_011516882.1:c.179T= XP_011515184.1:p.Ile60=
XR_928569.1:n.1020+19617A=
XR_928570.1:n.1020+19617A=
NM_001172815.2:c.179T= NP_001166286.1:p.Ile60=
XM_024447083.1:c.179T= XP_024302851.1:p.Ile60=
XR_928569.2:n.973+19617A=
XR_928570.2:n.973+19617A=
NM_001172811.2:c.179T= NP_001166282.1:p.Ile60=
NM_001172813.2:c.179T= NP_001166284.1:p.Ile60=
NM_001172814.2:c.179T= NP_001166285.1:p.Ile60=
NM_173851.3:c.326T= MANE Select NP_776250.2:p.Ile109=
NM_001172815.3:c.179T= NP_001166286.1:p.Ile60=