Canonical Allele Identifier: CA846188178

Gene: SLC30A8

Linked Data

• dbSNP Id: rs1326401123
• gnomAD v3: 8-117077348-G-GA
• gnomAD v4: 8-117077348-G-GA
• MyVariant Identifiers: chr8:g.118089587_118089588insA (hg19) ; chr8:g.117077348_117077349insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117077355dup , CM000670.2:g.117077355dup	GRCh38
NC_000008.10:g.118089594dup , CM000670.1:g.118089594dup	GRCh37
NC_000008.9:g.118158775dup	NCBI36
NG_016991.1:g.132083dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427715.2:c.-226+38097dup	ENSP00000407505.2:n.-226+38097dup
ENST00000521035.5:n.295-57877dup
ENST00000521243.5:c.-106-69464dup	ENSP00000428545.1:n.-106-69464dup
ENST00000524274.5:c.-106-69464dup	ENSP00000427760.1:n.-106-69464dup
NM_001172811.1:c.-106-69464dup	NP_001166282.1:n.-106-69464dup
NM_001172813.1:c.-273-57877dup	NP_001166284.1:n.-273-57877dup
NM_001172815.1:c.-226+38097dup	NP_001166286.1:n.-226+38097dup
XM_011516881.1:c.-96-57877dup	XP_011515183.1:n.-96-57877dup
NM_001172815.2:c.-226+38097dup	NP_001166286.1:n.-226+38097dup
XM_024447083.1:c.-106-69464dup	XP_024302851.1:n.-106-69464dup
NM_001172811.2:c.-106-69464dup	NP_001166282.1:n.-106-69464dup
NM_001172813.2:c.-273-57877dup	NP_001166284.1:n.-273-57877dup
NM_001172815.3:c.-226+38097dup	NP_001166286.1:n.-226+38097dup