Canonical Allele Identifier: CA2578075376
Gene: SLC30A9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42001562A>T , CM000666.2:g.42001562A>T GRCh38
NC_000004.11:g.42003579A>T , CM000666.1:g.42003579A>T GRCh37
NC_000004.10:g.41698336A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264451.12:c.110-54A>T MANE Select ENSP00000264451.6:n.110-54A>T
ENST00000264451.11:c.110-54A>T ENSP00000264451.6:n.110-54A>T
ENST00000510460.1:n.235-54A>T
ENST00000513699.5:c.110-54A>T ENSP00000423529.1:n.110-54A>T
NM_006345.3:c.110-54A>T NP_006336.3:n.110-54A>T
XM_011513620.1:c.110-54A>T XP_011511922.1:n.110-54A>T
XM_017007654.2:c.110-54A>T XP_016863143.1:n.110-54A>T
XR_001741095.2:n.260-54A>T
NM_006345.4:c.110-54A>T MANE Select NP_006336.3:n.110-54A>T
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