Canonical Allele Identifier: CA2670470477

Gene: SLC30A9

Linked Data

• gnomAD v4: 4-42001567-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42001567G>A , CM000666.2:g.42001567G>A	GRCh38
NC_000004.11:g.42003584G>A , CM000666.1:g.42003584G>A	GRCh37
NC_000004.10:g.41698341G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264451.12:c.110-49G>A MANE Select	ENSP00000264451.6:n.110-49G>A
ENST00000264451.11:c.110-49G>A	ENSP00000264451.6:n.110-49G>A
ENST00000510460.1:n.235-49G>A
ENST00000513699.5:c.110-49G>A	ENSP00000423529.1:n.110-49G>A
NM_006345.3:c.110-49G>A	NP_006336.3:n.110-49G>A
XM_011513620.1:c.110-49G>A	XP_011511922.1:n.110-49G>A
XM_017007654.2:c.110-49G>A	XP_016863143.1:n.110-49G>A
XR_001741095.2:n.260-49G>A
NM_006345.4:c.110-49G>A MANE Select	NP_006336.3:n.110-49G>A