Canonical Allele Identifier: CA2670470491
Gene: SLC30A9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42001602_42001603dup , CM000666.2:g.42001602_42001603dup GRCh38
NC_000004.11:g.42003619_42003620dup , CM000666.1:g.42003619_42003620dup GRCh37
NC_000004.10:g.41698376_41698377dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264451.12:c.110-14_110-13dup MANE Select ENSP00000264451.6:n.110-14_110-13dup
ENST00000264451.11:c.110-14_110-13dup ENSP00000264451.6:n.110-14_110-13dup
ENST00000510460.1:n.235-14_235-13dup
ENST00000513699.5:c.110-14_110-13dup ENSP00000423529.1:n.110-14_110-13dup
NM_006345.3:c.110-14_110-13dup NP_006336.3:n.110-14_110-13dup
XM_011513620.1:c.110-14_110-13dup XP_011511922.1:n.110-14_110-13dup
XM_017007654.2:c.110-14_110-13dup XP_016863143.1:n.110-14_110-13dup
XR_001741095.2:n.260-14_260-13dup
NM_006345.4:c.110-14_110-13dup MANE Select NP_006336.3:n.110-14_110-13dup