Canonical Allele Identifier: CA462469112

Gene: SLC30A8

Linked Data

• MyVariant Identifiers: chr8:g.118184854C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117172615C>T , CM000670.2:g.117172615C>T	GRCh38
NC_000008.10:g.118184854C>T , CM000670.1:g.118184854C>T	GRCh37
NC_000008.9:g.118254035C>T	NCBI36
NG_016991.1:g.227343C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.1044C>T MANE Select	ENSP00000415011.2:p.Thr348=
ENST00000427715.2:c.897C>T	ENSP00000407505.2:p.Thr299=
ENST00000456015.6:c.1044C>T	ENSP00000415011.2:p.Thr348=
ENST00000519688.5:c.897C>T	ENSP00000431069.1:p.Thr299=
ENST00000521243.5:c.897C>T	ENSP00000428545.1:p.Thr299=
NM_001172811.1:c.897C>T	NP_001166282.1:p.Thr299=
NM_001172813.1:c.897C>T	NP_001166284.1:p.Thr299=
NM_001172814.1:c.897C>T	NP_001166285.1:p.Thr299=
NM_001172815.1:c.897C>T	NP_001166286.1:p.Thr299=
NM_173851.2:c.1044C>T	NP_776250.2:p.Thr348=
XM_011516881.1:c.1044C>T	XP_011515183.1:p.Thr348=
XM_011516882.1:c.897C>T	XP_011515184.1:p.Thr299=
XR_928569.1:n.1020G>A
XR_928570.1:n.1020G>A
NM_001172815.2:c.897C>T	NP_001166286.1:p.Thr299=
XM_024447083.1:c.897C>T	XP_024302851.1:p.Thr299=
XR_928569.2:n.973G>A
XR_928570.2:n.973G>A
NM_001172811.2:c.897C>T	NP_001166282.1:p.Thr299=
NM_001172813.2:c.897C>T	NP_001166284.1:p.Thr299=
NM_001172814.2:c.897C>T	NP_001166285.1:p.Thr299=
NM_173851.3:c.1044C>T MANE Select	NP_776250.2:p.Thr348=
NM_001172815.3:c.897C>T	NP_001166286.1:p.Thr299=