Canonical Allele Identifier: CA2497076613
Gene: SLC30A9 HGNC NCBI

Linked Data

dbSNP Id: rs1714984548

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42001562_42001565dup , CM000666.2:g.42001562_42001565dup GRCh38
NC_000004.11:g.42003579_42003582dup , CM000666.1:g.42003579_42003582dup GRCh37
NC_000004.10:g.41698336_41698339dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264451.12:c.110-54_110-51dup MANE Select ENSP00000264451.6:n.110-54_110-51dup
ENST00000264451.11:c.110-54_110-51dup ENSP00000264451.6:n.110-54_110-51dup
ENST00000510460.1:n.235-54_235-51dup
ENST00000513699.5:c.110-54_110-51dup ENSP00000423529.1:n.110-54_110-51dup
NM_006345.3:c.110-54_110-51dup NP_006336.3:n.110-54_110-51dup
XM_011513620.1:c.110-54_110-51dup XP_011511922.1:n.110-54_110-51dup
XM_017007654.2:c.110-54_110-51dup XP_016863143.1:n.110-54_110-51dup
XR_001741095.2:n.260-54_260-51dup
NM_006345.4:c.110-54_110-51dup MANE Select NP_006336.3:n.110-54_110-51dup