Canonical Allele Identifier: CA584427796

Gene: SLC30A8

Linked Data

• dbSNP Id: rs1168043661
• gnomAD v2: 8-118154797-C-T
• gnomAD v3: 8-117142558-C-T
• gnomAD v4: 8-117142558-C-T
• MyVariant Identifiers: chr8:g.118154797C>T (hg19) ; chr8:g.117142558C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117142558C>T , CM000670.2:g.117142558C>T	GRCh38
NC_000008.10:g.118154797C>T , CM000670.1:g.118154797C>T	GRCh37
NC_000008.9:g.118223978C>T	NCBI36
NG_016991.1:g.197286C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.72-4396C>T MANE Select	ENSP00000415011.2:n.72-4396C>T
ENST00000427715.2:c.-106-4261C>T	ENSP00000407505.2:n.-106-4261C>T
ENST00000456015.6:c.72-4396C>T	ENSP00000415011.2:n.72-4396C>T
ENST00000518396.5:c.-106-4261C>T	ENSP00000485167.1:n.-106-4261C>T
ENST00000518521.5:c.-76-4396C>T	ENSP00000485566.1:n.-76-4396C>T
ENST00000519688.5:c.-106-4261C>T	ENSP00000431069.1:n.-106-4261C>T
ENST00000520469.1:n.326-4396C>T
ENST00000521035.5:n.462-4261C>T
ENST00000521243.5:c.-106-4261C>T	ENSP00000428545.1:n.-106-4261C>T
ENST00000524274.5:c.-106-4261C>T	ENSP00000427760.1:n.-106-4261C>T
NM_001172811.1:c.-106-4261C>T	NP_001166282.1:n.-106-4261C>T
NM_001172813.1:c.-106-4261C>T	NP_001166284.1:n.-106-4261C>T
NM_001172814.1:c.-106-4261C>T	NP_001166285.1:n.-106-4261C>T
NM_001172815.1:c.-106-4261C>T	NP_001166286.1:n.-106-4261C>T
NM_173851.2:c.72-4396C>T	NP_776250.2:n.72-4396C>T
XM_011516881.1:c.72-4396C>T	XP_011515183.1:n.72-4396C>T
XR_928569.1:n.1020+30057G>A
XR_928570.1:n.1021-24772G>A
NM_001172815.2:c.-106-4261C>T	NP_001166286.1:n.-106-4261C>T
XM_024447083.1:c.-106-4261C>T	XP_024302851.1:n.-106-4261C>T
XR_928569.2:n.973+30057G>A
XR_928570.2:n.974-24772G>A
NM_001172811.2:c.-106-4261C>T	NP_001166282.1:n.-106-4261C>T
NM_001172813.2:c.-106-4261C>T	NP_001166284.1:n.-106-4261C>T
NM_001172814.2:c.-106-4261C>T	NP_001166285.1:n.-106-4261C>T
NM_173851.3:c.72-4396C>T MANE Select	NP_776250.2:n.72-4396C>T
NM_001172815.3:c.-106-4261C>T	NP_001166286.1:n.-106-4261C>T