Canonical Allele Identifier: CA1813628953

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117151143T= , CM000670.2:g.117151143T=	GRCh38
NC_000008.10:g.118163382T= , CM000670.1:g.118163382T=	GRCh37
NC_000008.9:g.118232563T=	NCBI36
NG_016991.1:g.205871T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.272-1801T= MANE Select	ENSP00000415011.2:n.272-1801T=
ENST00000427715.2:c.125-1801T=	ENSP00000407505.2:n.125-1801T=
ENST00000456015.6:c.272-1801T=	ENSP00000415011.2:n.272-1801T=
ENST00000518521.5:c.125-1801T=	ENSP00000485566.1:n.125-1801T=
ENST00000519688.5:c.125-1801T=	ENSP00000431069.1:n.125-1801T=
ENST00000521243.5:c.125-1801T=	ENSP00000428545.1:n.125-1801T=
ENST00000524274.5:c.125-1801T=	ENSP00000427760.1:n.125-1801T=
NM_001172811.1:c.125-1801T=	NP_001166282.1:n.125-1801T=
NM_001172813.1:c.125-1801T=	NP_001166284.1:n.125-1801T=
NM_001172814.1:c.125-1801T=	NP_001166285.1:n.125-1801T=
NM_001172815.1:c.125-1801T=	NP_001166286.1:n.125-1801T=
NM_173851.2:c.272-1801T=	NP_776250.2:n.272-1801T=
XM_011516881.1:c.272-1801T=	XP_011515183.1:n.272-1801T=
XM_011516882.1:c.125-1801T=	XP_011515184.1:n.125-1801T=
XR_928569.1:n.1020+21472A=
XR_928570.1:n.1020+21472A=
NM_001172815.2:c.125-1801T=	NP_001166286.1:n.125-1801T=
XM_024447083.1:c.125-1801T=	XP_024302851.1:n.125-1801T=
XR_928569.2:n.973+21472A=
XR_928570.2:n.973+21472A=
NM_001172811.2:c.125-1801T=	NP_001166282.1:n.125-1801T=
NM_001172813.2:c.125-1801T=	NP_001166284.1:n.125-1801T=
NM_001172814.2:c.125-1801T=	NP_001166285.1:n.125-1801T=
NM_173851.3:c.272-1801T= MANE Select	NP_776250.2:n.272-1801T=
NM_001172815.3:c.125-1801T=	NP_001166286.1:n.125-1801T=