Canonical Allele Identifier: CA462469045

Gene: SLC30A8

Linked Data

• MyVariant Identifiers: chr8:g.118184794A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117172555A>G , CM000670.2:g.117172555A>G	GRCh38
NC_000008.10:g.118184794A>G , CM000670.1:g.118184794A>G	GRCh37
NC_000008.9:g.118253975A>G	NCBI36
NG_016991.1:g.227283A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.984A>G MANE Select	ENSP00000415011.2:p.Gln328=
ENST00000427715.2:c.837A>G	ENSP00000407505.2:p.Gln279=
ENST00000456015.6:c.984A>G	ENSP00000415011.2:p.Gln328=
ENST00000519688.5:c.837A>G	ENSP00000431069.1:p.Gln279=
ENST00000521243.5:c.837A>G	ENSP00000428545.1:p.Gln279=
NM_001172811.1:c.837A>G	NP_001166282.1:p.Gln279=
NM_001172813.1:c.837A>G	NP_001166284.1:p.Gln279=
NM_001172814.1:c.837A>G	NP_001166285.1:p.Gln279=
NM_001172815.1:c.837A>G	NP_001166286.1:p.Gln279=
NM_173851.2:c.984A>G	NP_776250.2:p.Gln328=
XM_011516881.1:c.984A>G	XP_011515183.1:p.Gln328=
XM_011516882.1:c.837A>G	XP_011515184.1:p.Gln279=
XR_928569.1:n.1020+60T>C
XR_928570.1:n.1020+60T>C
NM_001172815.2:c.837A>G	NP_001166286.1:p.Gln279=
XM_024447083.1:c.837A>G	XP_024302851.1:p.Gln279=
XR_928569.2:n.973+60T>C
XR_928570.2:n.973+60T>C
NM_001172811.2:c.837A>G	NP_001166282.1:p.Gln279=
NM_001172813.2:c.837A>G	NP_001166284.1:p.Gln279=
NM_001172814.2:c.837A>G	NP_001166285.1:p.Gln279=
NM_173851.3:c.984A>G MANE Select	NP_776250.2:p.Gln328=
NM_001172815.3:c.837A>G	NP_001166286.1:p.Gln279=