Canonical Allele Identifier: CA462465090

Gene: SLC30A8

Linked Data

• MyVariant Identifiers: chr8:g.118165295C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117153056C>A , CM000670.2:g.117153056C>A	GRCh38
NC_000008.10:g.118165295C>A , CM000670.1:g.118165295C>A	GRCh37
NC_000008.9:g.118234476C>A	NCBI36
NG_016991.1:g.207784C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.384C>A MANE Select	ENSP00000415011.2:p.Pro128=
ENST00000427715.2:c.237C>A	ENSP00000407505.2:p.Pro79=
ENST00000456015.6:c.384C>A	ENSP00000415011.2:p.Pro128=
ENST00000519688.5:c.237C>A	ENSP00000431069.1:p.Pro79=
ENST00000521243.5:c.237C>A	ENSP00000428545.1:p.Pro79=
ENST00000524274.5:c.237C>A	ENSP00000427760.1:p.Pro79=
NM_001172811.1:c.237C>A	NP_001166282.1:p.Pro79=
NM_001172813.1:c.237C>A	NP_001166284.1:p.Pro79=
NM_001172814.1:c.237C>A	NP_001166285.1:p.Pro79=
NM_001172815.1:c.237C>A	NP_001166286.1:p.Pro79=
NM_173851.2:c.384C>A	NP_776250.2:p.Pro128=
XM_011516881.1:c.384C>A	XP_011515183.1:p.Pro128=
XM_011516882.1:c.237C>A	XP_011515184.1:p.Pro79=
XR_928569.1:n.1020+19559G>T
XR_928570.1:n.1020+19559G>T
NM_001172815.2:c.237C>A	NP_001166286.1:p.Pro79=
XM_024447083.1:c.237C>A	XP_024302851.1:p.Pro79=
XR_928569.2:n.973+19559G>T
XR_928570.2:n.973+19559G>T
NM_001172811.2:c.237C>A	NP_001166282.1:p.Pro79=
NM_001172813.2:c.237C>A	NP_001166284.1:p.Pro79=
NM_001172814.2:c.237C>A	NP_001166285.1:p.Pro79=
NM_173851.3:c.384C>A MANE Select	NP_776250.2:p.Pro128=
NM_001172815.3:c.237C>A	NP_001166286.1:p.Pro79=