Canonical Allele Identifier: CA1813659267

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117172457A= , CM000670.2:g.117172457A=	GRCh38
NC_000008.10:g.118184696A= , CM000670.1:g.118184696A=	GRCh37
NC_000008.9:g.118253877A=	NCBI36
NG_016991.1:g.227185A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.965-79A= MANE Select	ENSP00000415011.2:n.965-79A=
ENST00000427715.2:c.818-79A=	ENSP00000407505.2:n.818-79A=
ENST00000456015.6:c.965-79A=	ENSP00000415011.2:n.965-79A=
ENST00000519688.5:c.818-79A=	ENSP00000431069.1:n.818-79A=
ENST00000521243.5:c.818-79A=	ENSP00000428545.1:n.818-79A=
NM_001172811.1:c.818-79A=	NP_001166282.1:n.818-79A=
NM_001172813.1:c.818-79A=	NP_001166284.1:n.818-79A=
NM_001172814.1:c.818-79A=	NP_001166285.1:n.818-79A=
NM_001172815.1:c.818-79A=	NP_001166286.1:n.818-79A=
NM_173851.2:c.965-79A=	NP_776250.2:n.965-79A=
XM_011516881.1:c.965-79A=	XP_011515183.1:n.965-79A=
XM_011516882.1:c.818-79A=	XP_011515184.1:n.818-79A=
XR_928569.1:n.1020+158T=
XR_928570.1:n.1020+158T=
NM_001172815.2:c.818-79A=	NP_001166286.1:n.818-79A=
XM_024447083.1:c.818-79A=	XP_024302851.1:n.818-79A=
XR_928569.2:n.973+158T=
XR_928570.2:n.973+158T=
NM_001172811.2:c.818-79A=	NP_001166282.1:n.818-79A=
NM_001172813.2:c.818-79A=	NP_001166284.1:n.818-79A=
NM_001172814.2:c.818-79A=	NP_001166285.1:n.818-79A=
NM_173851.3:c.965-79A= MANE Select	NP_776250.2:n.965-79A=
NM_001172815.3:c.818-79A=	NP_001166286.1:n.818-79A=