Canonical Allele Identifier: CA371910099

Gene: SLC30A8

Linked Data

• gnomAD v4: 8-117153070-C-T
• MyVariant Identifiers: chr8:g.118165309C>T (hg19) ; chr8:g.117153070C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117153070C>T , CM000670.2:g.117153070C>T	GRCh38
NC_000008.10:g.118165309C>T , CM000670.1:g.118165309C>T	GRCh37
NC_000008.9:g.118234490C>T	NCBI36
NG_016991.1:g.207798C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.398C>T MANE Select	ENSP00000415011.2:p.Thr133Ile
ENST00000427715.2:c.251C>T	ENSP00000407505.2:p.Thr84Ile
ENST00000456015.6:c.398C>T	ENSP00000415011.2:p.Thr133Ile
ENST00000519688.5:c.251C>T	ENSP00000431069.1:p.Thr84Ile
ENST00000521243.5:c.251C>T	ENSP00000428545.1:p.Thr84Ile
ENST00000524274.5:c.251C>T	ENSP00000427760.1:p.Thr84Ile
NM_001172811.1:c.251C>T	NP_001166282.1:p.Thr84Ile
NM_001172813.1:c.251C>T	NP_001166284.1:p.Thr84Ile
NM_001172814.1:c.251C>T	NP_001166285.1:p.Thr84Ile
NM_001172815.1:c.251C>T	NP_001166286.1:p.Thr84Ile
NM_173851.2:c.398C>T	NP_776250.2:p.Thr133Ile
XM_011516881.1:c.398C>T	XP_011515183.1:p.Thr133Ile
XM_011516882.1:c.251C>T	XP_011515184.1:p.Thr84Ile
XR_928569.1:n.1020+19545G>A
XR_928570.1:n.1020+19545G>A
NM_001172815.2:c.251C>T	NP_001166286.1:p.Thr84Ile
XM_024447083.1:c.251C>T	XP_024302851.1:p.Thr84Ile
XR_928569.2:n.973+19545G>A
XR_928570.2:n.973+19545G>A
NM_001172811.2:c.251C>T	NP_001166282.1:p.Thr84Ile
NM_001172813.2:c.251C>T	NP_001166284.1:p.Thr84Ile
NM_001172814.2:c.251C>T	NP_001166285.1:p.Thr84Ile
NM_173851.3:c.398C>T MANE Select	NP_776250.2:p.Thr133Ile
NM_001172815.3:c.251C>T	NP_001166286.1:p.Thr84Ile