Canonical Allele Identifier: CA95845445
Gene: SLC30A9 HGNC NCBI

Linked Data

dbSNP Id: rs1013435063

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42001593del , CM000666.2:g.42001593del GRCh38
NC_000004.11:g.42003610del , CM000666.1:g.42003610del GRCh37
NC_000004.10:g.41698367del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264451.12:c.110-23del MANE Select ENSP00000264451.6:n.110-23del
ENST00000264451.11:c.110-23del ENSP00000264451.6:n.110-23del
ENST00000510460.1:n.235-23del
ENST00000513699.5:c.110-23del ENSP00000423529.1:n.110-23del
NM_006345.3:c.110-23del NP_006336.3:n.110-23del
XM_011513620.1:c.110-23del XP_011511922.1:n.110-23del
XM_017007654.2:c.110-23del XP_016863143.1:n.110-23del
XR_001741095.2:n.260-23del
NM_006345.4:c.110-23del MANE Select NP_006336.3:n.110-23del