Canonical Allele Identifier: CA1813625406

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117142766G= , CM000670.2:g.117142766G=	GRCh38
NC_000008.10:g.118155005G= , CM000670.1:g.118155005G=	GRCh37
NC_000008.9:g.118224186G=	NCBI36
NG_016991.1:g.197494G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.72-4188G= MANE Select	ENSP00000415011.2:n.72-4188G=
ENST00000427715.2:c.-106-4053G=	ENSP00000407505.2:n.-106-4053G=
ENST00000456015.6:c.72-4188G=	ENSP00000415011.2:n.72-4188G=
ENST00000518396.5:c.-106-4053G=	ENSP00000485167.1:n.-106-4053G=
ENST00000518521.5:c.-76-4188G=	ENSP00000485566.1:n.-76-4188G=
ENST00000519688.5:c.-106-4053G=	ENSP00000431069.1:n.-106-4053G=
ENST00000520469.1:n.326-4188G=
ENST00000521035.5:n.462-4053G=
ENST00000521243.5:c.-106-4053G=	ENSP00000428545.1:n.-106-4053G=
ENST00000524274.5:c.-106-4053G=	ENSP00000427760.1:n.-106-4053G=
NM_001172811.1:c.-106-4053G=	NP_001166282.1:n.-106-4053G=
NM_001172813.1:c.-106-4053G=	NP_001166284.1:n.-106-4053G=
NM_001172814.1:c.-106-4053G=	NP_001166285.1:n.-106-4053G=
NM_001172815.1:c.-106-4053G=	NP_001166286.1:n.-106-4053G=
NM_173851.2:c.72-4188G=	NP_776250.2:n.72-4188G=
XM_011516881.1:c.72-4188G=	XP_011515183.1:n.72-4188G=
XR_928569.1:n.1020+29849C=
XR_928570.1:n.1021-24980C=
NM_001172815.2:c.-106-4053G=	NP_001166286.1:n.-106-4053G=
XM_024447083.1:c.-106-4053G=	XP_024302851.1:n.-106-4053G=
XR_928569.2:n.973+29849C=
XR_928570.2:n.974-24980C=
NM_001172811.2:c.-106-4053G=	NP_001166282.1:n.-106-4053G=
NM_001172813.2:c.-106-4053G=	NP_001166284.1:n.-106-4053G=
NM_001172814.2:c.-106-4053G=	NP_001166285.1:n.-106-4053G=
NM_173851.3:c.72-4188G= MANE Select	NP_776250.2:n.72-4188G=
NM_001172815.3:c.-106-4053G=	NP_001166286.1:n.-106-4053G=