Canonical Allele Identifier: CA1813629834
Gene: SLC30A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117153094C= , CM000670.2:g.117153094C= GRCh38
NC_000008.10:g.118165333C= , CM000670.1:g.118165333C= GRCh37
NC_000008.9:g.118234514C= NCBI36
NG_016991.1:g.207822C=

Transcript Alleles

HGVS Amino-acid change
ENST00000456015.7:c.418+4C= MANE Select ENSP00000415011.2:n.418+4C=
ENST00000427715.2:c.271+4C= ENSP00000407505.2:n.271+4C=
ENST00000456015.6:c.418+4C= ENSP00000415011.2:n.418+4C=
ENST00000519688.5:c.271+4C= ENSP00000431069.1:n.271+4C=
ENST00000521243.5:c.271+4C= ENSP00000428545.1:n.271+4C=
NM_001172811.1:c.271+4C= NP_001166282.1:n.271+4C=
NM_001172813.1:c.271+4C= NP_001166284.1:n.271+4C=
NM_001172814.1:c.271+4C= NP_001166285.1:n.271+4C=
NM_001172815.1:c.271+4C= NP_001166286.1:n.271+4C=
NM_173851.2:c.418+4C= NP_776250.2:n.418+4C=
XM_011516881.1:c.418+4C= XP_011515183.1:n.418+4C=
XM_011516882.1:c.271+4C= XP_011515184.1:n.271+4C=
XR_928569.1:n.1020+19521G=
XR_928570.1:n.1020+19521G=
NM_001172815.2:c.271+4C= NP_001166286.1:n.271+4C=
XM_024447083.1:c.271+4C= XP_024302851.1:n.271+4C=
XR_928569.2:n.973+19521G=
XR_928570.2:n.973+19521G=
NM_001172811.2:c.271+4C= NP_001166282.1:n.271+4C=
NM_001172813.2:c.271+4C= NP_001166284.1:n.271+4C=
NM_001172814.2:c.271+4C= NP_001166285.1:n.271+4C=
NM_173851.3:c.418+4C= MANE Select NP_776250.2:n.418+4C=
NM_001172815.3:c.271+4C= NP_001166286.1:n.271+4C=