Canonical Allele Identifier: CA1813659709

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117173442C= , CM000670.2:g.117173442C=	GRCh38
NC_000008.10:g.118185681C= , CM000670.1:g.118185681C=	GRCh37
NC_000008.9:g.118254862C=	NCBI36
NG_016991.1:g.228170C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.*761C= MANE Select	ENSP00000415011.2:n.*761C=
ENST00000427715.2:c.*761C=	ENSP00000407505.2:n.*761C=
ENST00000456015.6:c.1871C=	ENSP00000415011.2:n.1871C=
ENST00000519688.5:c.*761C=	ENSP00000431069.1:n.*761C=
NM_001172811.1:c.*761C=	NP_001166282.1:n.*761C=
NM_001172813.1:c.*761C=	NP_001166284.1:n.*761C=
NM_001172814.1:c.*761C=	NP_001166285.1:n.*761C=
NM_001172815.1:c.*761C=	NP_001166286.1:n.*761C=
NM_173851.2:c.*761C=	NP_776250.2:n.*761C=
XM_011516881.1:c.*761C=	XP_011515183.1:n.*761C=
XM_011516882.1:c.*761C=	XP_011515184.1:n.*761C=
XR_928566.1:n.966G=
XR_928567.1:n.559G=
XR_928568.1:n.764G=
XR_928569.1:n.807G=
XR_928570.1:n.807G=
NM_001172815.2:c.*761C=	NP_001166286.1:n.*761C=
XM_024447083.1:c.*761C=	XP_024302851.1:n.*761C=
XR_001746038.1:n.751G=
XR_928566.2:n.909G=
XR_928567.2:n.522G=
XR_928568.3:n.762G=
XR_928569.2:n.760G=
XR_928570.2:n.760G=
NM_001172811.2:c.*761C=	NP_001166282.1:n.*761C=
NM_001172813.2:c.*761C=	NP_001166284.1:n.*761C=
NM_001172814.2:c.*761C=	NP_001166285.1:n.*761C=
NM_173851.3:c.*761C= MANE Select	NP_776250.2:n.*761C=
NM_001172815.3:c.*761C=	NP_001166286.1:n.*761C=