Canonical Allele Identifier: CA2688340633

Gene: SLC30A8

Linked Data

• gnomAD v4: 8-117173462-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117173462G>T , CM000670.2:g.117173462G>T	GRCh38
NC_000008.10:g.118185701G>T , CM000670.1:g.118185701G>T	GRCh37
NC_000008.9:g.118254882G>T	NCBI36
NG_016991.1:g.228190G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.*781G>T MANE Select	ENSP00000415011.2:n.*781G>T
ENST00000427715.2:c.*781G>T	ENSP00000407505.2:n.*781G>T
ENST00000456015.6:c.1891G>T	ENSP00000415011.2:n.1891G>T
ENST00000519688.5:c.*781G>T	ENSP00000431069.1:n.*781G>T
NM_001172811.1:c.*781G>T	NP_001166282.1:n.*781G>T
NM_001172813.1:c.*781G>T	NP_001166284.1:n.*781G>T
NM_001172814.1:c.*781G>T	NP_001166285.1:n.*781G>T
NM_001172815.1:c.*781G>T	NP_001166286.1:n.*781G>T
NM_173851.2:c.*781G>T	NP_776250.2:n.*781G>T
XM_011516881.1:c.*781G>T	XP_011515183.1:n.*781G>T
XM_011516882.1:c.*781G>T	XP_011515184.1:n.*781G>T
XR_928566.1:n.946C>A
XR_928567.1:n.539C>A
XR_928568.1:n.744C>A
XR_928569.1:n.787C>A
XR_928570.1:n.787C>A
NM_001172815.2:c.*781G>T	NP_001166286.1:n.*781G>T
XM_024447083.1:c.*781G>T	XP_024302851.1:n.*781G>T
XR_001746038.1:n.731C>A
XR_928566.2:n.889C>A
XR_928567.2:n.502C>A
XR_928568.3:n.742C>A
XR_928569.2:n.740C>A
XR_928570.2:n.740C>A
NM_001172811.2:c.*781G>T	NP_001166282.1:n.*781G>T
NM_001172813.2:c.*781G>T	NP_001166284.1:n.*781G>T
NM_001172814.2:c.*781G>T	NP_001166285.1:n.*781G>T
NM_173851.3:c.*781G>T MANE Select	NP_776250.2:n.*781G>T
NM_001172815.3:c.*781G>T	NP_001166286.1:n.*781G>T