Canonical Allele Identifier: CA462465019

Gene: SLC30A8

Linked Data

• MyVariant Identifiers: chr8:g.118165208T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117152969T>C , CM000670.2:g.117152969T>C	GRCh38
NC_000008.10:g.118165208T>C , CM000670.1:g.118165208T>C	GRCh37
NC_000008.9:g.118234389T>C	NCBI36
NG_016991.1:g.207697T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.297T>C MANE Select	ENSP00000415011.2:p.Ala99=
ENST00000427715.2:c.150T>C	ENSP00000407505.2:p.Ala50=
ENST00000456015.6:c.297T>C	ENSP00000415011.2:p.Ala99=
ENST00000518521.5:c.150T>C	ENSP00000485566.1:p.Ala50=
ENST00000519688.5:c.150T>C	ENSP00000431069.1:p.Ala50=
ENST00000521243.5:c.150T>C	ENSP00000428545.1:p.Ala50=
ENST00000524274.5:c.150T>C	ENSP00000427760.1:p.Ala50=
NM_001172811.1:c.150T>C	NP_001166282.1:p.Ala50=
NM_001172813.1:c.150T>C	NP_001166284.1:p.Ala50=
NM_001172814.1:c.150T>C	NP_001166285.1:p.Ala50=
NM_001172815.1:c.150T>C	NP_001166286.1:p.Ala50=
NM_173851.2:c.297T>C	NP_776250.2:p.Ala99=
XM_011516881.1:c.297T>C	XP_011515183.1:p.Ala99=
XM_011516882.1:c.150T>C	XP_011515184.1:p.Ala50=
XR_928569.1:n.1020+19646A>G
XR_928570.1:n.1020+19646A>G
NM_001172815.2:c.150T>C	NP_001166286.1:p.Ala50=
XM_024447083.1:c.150T>C	XP_024302851.1:p.Ala50=
XR_928569.2:n.973+19646A>G
XR_928570.2:n.973+19646A>G
NM_001172811.2:c.150T>C	NP_001166282.1:p.Ala50=
NM_001172813.2:c.150T>C	NP_001166284.1:p.Ala50=
NM_001172814.2:c.150T>C	NP_001166285.1:p.Ala50=
NM_173851.3:c.297T>C MANE Select	NP_776250.2:p.Ala99=
NM_001172815.3:c.150T>C	NP_001166286.1:p.Ala50=