Canonical Allele Identifier: CA1813659797

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117173670C= , CM000670.2:g.117173670C=	GRCh38
NC_000008.10:g.118185909C= , CM000670.1:g.118185909C=	GRCh37
NC_000008.9:g.118255090C=	NCBI36
NG_016991.1:g.228398C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.*989C= MANE Select	ENSP00000415011.2:n.*989C=
ENST00000427715.2:c.*989C=	ENSP00000407505.2:n.*989C=
ENST00000456015.6:c.2099C=	ENSP00000415011.2:n.2099C=
ENST00000519688.5:c.*989C=	ENSP00000431069.1:n.*989C=
NM_001172811.1:c.*989C=	NP_001166282.1:n.*989C=
NM_001172813.1:c.*989C=	NP_001166284.1:n.*989C=
NM_001172814.1:c.*989C=	NP_001166285.1:n.*989C=
NM_001172815.1:c.*989C=	NP_001166286.1:n.*989C=
NM_173851.2:c.*989C=	NP_776250.2:n.*989C=
XM_011516881.1:c.*989C=	XP_011515183.1:n.*989C=
XM_011516882.1:c.*989C=	XP_011515184.1:n.*989C=
XR_928566.1:n.920-182G=
XR_928567.1:n.513-182G=
XR_928568.1:n.718-182G=
XR_928569.1:n.761-182G=
XR_928570.1:n.761-182G=
NM_001172815.2:c.*989C=	NP_001166286.1:n.*989C=
XM_024447083.1:c.*989C=	XP_024302851.1:n.*989C=
XR_001746038.1:n.705-182G=
XR_928566.2:n.863-182G=
XR_928567.2:n.476-182G=
XR_928568.3:n.716-182G=
XR_928569.2:n.714-182G=
XR_928570.2:n.714-182G=
NM_001172811.2:c.*989C=	NP_001166282.1:n.*989C=
NM_001172813.2:c.*989C=	NP_001166284.1:n.*989C=
NM_001172814.2:c.*989C=	NP_001166285.1:n.*989C=
NM_173851.3:c.*989C= MANE Select	NP_776250.2:n.*989C=
NM_001172815.3:c.*989C=	NP_001166286.1:n.*989C=