Canonical Allele Identifier: CA2688340630

Gene: SLC30A8

Linked Data

• gnomAD v4: 8-117173452-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117173452C>T , CM000670.2:g.117173452C>T	GRCh38
NC_000008.10:g.118185691C>T , CM000670.1:g.118185691C>T	GRCh37
NC_000008.9:g.118254872C>T	NCBI36
NG_016991.1:g.228180C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.*771C>T MANE Select	ENSP00000415011.2:n.*771C>T
ENST00000427715.2:c.*771C>T	ENSP00000407505.2:n.*771C>T
ENST00000456015.6:c.1881C>T	ENSP00000415011.2:n.1881C>T
ENST00000519688.5:c.*771C>T	ENSP00000431069.1:n.*771C>T
NM_001172811.1:c.*771C>T	NP_001166282.1:n.*771C>T
NM_001172813.1:c.*771C>T	NP_001166284.1:n.*771C>T
NM_001172814.1:c.*771C>T	NP_001166285.1:n.*771C>T
NM_001172815.1:c.*771C>T	NP_001166286.1:n.*771C>T
NM_173851.2:c.*771C>T	NP_776250.2:n.*771C>T
XM_011516881.1:c.*771C>T	XP_011515183.1:n.*771C>T
XM_011516882.1:c.*771C>T	XP_011515184.1:n.*771C>T
XR_928566.1:n.956G>A
XR_928567.1:n.549G>A
XR_928568.1:n.754G>A
XR_928569.1:n.797G>A
XR_928570.1:n.797G>A
NM_001172815.2:c.*771C>T	NP_001166286.1:n.*771C>T
XM_024447083.1:c.*771C>T	XP_024302851.1:n.*771C>T
XR_001746038.1:n.741G>A
XR_928566.2:n.899G>A
XR_928567.2:n.512G>A
XR_928568.3:n.752G>A
XR_928569.2:n.750G>A
XR_928570.2:n.750G>A
NM_001172811.2:c.*771C>T	NP_001166282.1:n.*771C>T
NM_001172813.2:c.*771C>T	NP_001166284.1:n.*771C>T
NM_001172814.2:c.*771C>T	NP_001166285.1:n.*771C>T
NM_173851.3:c.*771C>T MANE Select	NP_776250.2:n.*771C>T
NM_001172815.3:c.*771C>T	NP_001166286.1:n.*771C>T