Canonical Allele Identifier: CA1813659706

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117173432C= , CM000670.2:g.117173432C=	GRCh38
NC_000008.10:g.118185671C= , CM000670.1:g.118185671C=	GRCh37
NC_000008.9:g.118254852C=	NCBI36
NG_016991.1:g.228160C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.*751C= MANE Select	ENSP00000415011.2:n.*751C=
ENST00000427715.2:c.*751C=	ENSP00000407505.2:n.*751C=
ENST00000456015.6:c.1861C=	ENSP00000415011.2:n.1861C=
ENST00000519688.5:c.*751C=	ENSP00000431069.1:n.*751C=
NM_001172811.1:c.*751C=	NP_001166282.1:n.*751C=
NM_001172813.1:c.*751C=	NP_001166284.1:n.*751C=
NM_001172814.1:c.*751C=	NP_001166285.1:n.*751C=
NM_001172815.1:c.*751C=	NP_001166286.1:n.*751C=
NM_173851.2:c.*751C=	NP_776250.2:n.*751C=
XM_011516881.1:c.*751C=	XP_011515183.1:n.*751C=
XM_011516882.1:c.*751C=	XP_011515184.1:n.*751C=
XR_928566.1:n.976G=
XR_928567.1:n.569G=
XR_928568.1:n.774G=
XR_928569.1:n.817G=
XR_928570.1:n.817G=
NM_001172815.2:c.*751C=	NP_001166286.1:n.*751C=
XM_024447083.1:c.*751C=	XP_024302851.1:n.*751C=
XR_001746038.1:n.761G=
XR_928566.2:n.919G=
XR_928567.2:n.532G=
XR_928568.3:n.772G=
XR_928569.2:n.770G=
XR_928570.2:n.770G=
NM_001172811.2:c.*751C=	NP_001166282.1:n.*751C=
NM_001172813.2:c.*751C=	NP_001166284.1:n.*751C=
NM_001172814.2:c.*751C=	NP_001166285.1:n.*751C=
NM_173851.3:c.*751C= MANE Select	NP_776250.2:n.*751C=
NM_001172815.3:c.*751C=	NP_001166286.1:n.*751C=