Canonical Allele Identifier: CA2568846085
Gene: SLC30A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117151142A>C , CM000670.2:g.117151142A>C GRCh38
NC_000008.10:g.118163381A>C , CM000670.1:g.118163381A>C GRCh37
NC_000008.9:g.118232562A>C NCBI36
NG_016991.1:g.205870A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000456015.7:c.272-1802A>C MANE Select ENSP00000415011.2:n.272-1802A>C
ENST00000427715.2:c.125-1802A>C ENSP00000407505.2:n.125-1802A>C
ENST00000456015.6:c.272-1802A>C ENSP00000415011.2:n.272-1802A>C
ENST00000518521.5:c.125-1802A>C ENSP00000485566.1:n.125-1802A>C
ENST00000519688.5:c.125-1802A>C ENSP00000431069.1:n.125-1802A>C
ENST00000521243.5:c.125-1802A>C ENSP00000428545.1:n.125-1802A>C
ENST00000524274.5:c.125-1802A>C ENSP00000427760.1:n.125-1802A>C
NM_001172811.1:c.125-1802A>C NP_001166282.1:n.125-1802A>C
NM_001172813.1:c.125-1802A>C NP_001166284.1:n.125-1802A>C
NM_001172814.1:c.125-1802A>C NP_001166285.1:n.125-1802A>C
NM_001172815.1:c.125-1802A>C NP_001166286.1:n.125-1802A>C
NM_173851.2:c.272-1802A>C NP_776250.2:n.272-1802A>C
XM_011516881.1:c.272-1802A>C XP_011515183.1:n.272-1802A>C
XM_011516882.1:c.125-1802A>C XP_011515184.1:n.125-1802A>C
XR_928569.1:n.1020+21473T>G
XR_928570.1:n.1020+21473T>G
NM_001172815.2:c.125-1802A>C NP_001166286.1:n.125-1802A>C
XM_024447083.1:c.125-1802A>C XP_024302851.1:n.125-1802A>C
XR_928569.2:n.973+21473T>G
XR_928570.2:n.973+21473T>G
NM_001172811.2:c.125-1802A>C NP_001166282.1:n.125-1802A>C
NM_001172813.2:c.125-1802A>C NP_001166284.1:n.125-1802A>C
NM_001172814.2:c.125-1802A>C NP_001166285.1:n.125-1802A>C
NM_173851.3:c.272-1802A>C MANE Select NP_776250.2:n.272-1802A>C
NM_001172815.3:c.125-1802A>C NP_001166286.1:n.125-1802A>C