Canonical Allele Identifier: CA2578075379
Gene: SLC30A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42001592A>G , CM000666.2:g.42001592A>G GRCh38
NC_000004.11:g.42003609A>G , CM000666.1:g.42003609A>G GRCh37
NC_000004.10:g.41698366A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264451.12:c.110-24A>G MANE Select ENSP00000264451.6:n.110-24A>G
ENST00000264451.11:c.110-24A>G ENSP00000264451.6:n.110-24A>G
ENST00000510460.1:n.235-24A>G
ENST00000513699.5:c.110-24A>G ENSP00000423529.1:n.110-24A>G
NM_006345.3:c.110-24A>G NP_006336.3:n.110-24A>G
XM_011513620.1:c.110-24A>G XP_011511922.1:n.110-24A>G
XM_017007654.2:c.110-24A>G XP_016863143.1:n.110-24A>G
XR_001741095.2:n.260-24A>G
NM_006345.4:c.110-24A>G MANE Select NP_006336.3:n.110-24A>G