Canonical Allele Identifier: CA1813622877

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117138614T= , CM000670.2:g.117138614T=	GRCh38
NC_000008.10:g.118150853T= , CM000670.1:g.118150853T=	GRCh37
NC_000008.9:g.118220034T=	NCBI36
NG_016991.1:g.193342T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.71+3216T= MANE Select	ENSP00000415011.2:n.71+3216T=
ENST00000427715.2:c.-107+3216T=	ENSP00000407505.2:n.-107+3216T=
ENST00000456015.6:c.71+3216T=	ENSP00000415011.2:n.71+3216T=
ENST00000518396.5:c.-107+3216T=	ENSP00000485167.1:n.-107+3216T=
ENST00000518521.5:c.-77+3216T=	ENSP00000485566.1:n.-77+3216T=
ENST00000519688.5:c.-107+3216T=	ENSP00000431069.1:n.-107+3216T=
ENST00000520469.1:n.325+3216T=
ENST00000521035.5:n.461+3216T=
ENST00000521243.5:c.-106-8205T=	ENSP00000428545.1:n.-106-8205T=
ENST00000524274.5:c.-106-8205T=	ENSP00000427760.1:n.-106-8205T=
NM_001172811.1:c.-106-8205T=	NP_001166282.1:n.-106-8205T=
NM_001172813.1:c.-107+3216T=	NP_001166284.1:n.-107+3216T=
NM_001172814.1:c.-107+3216T=	NP_001166285.1:n.-107+3216T=
NM_001172815.1:c.-107+3216T=	NP_001166286.1:n.-107+3216T=
NM_173851.2:c.71+3216T=	NP_776250.2:n.71+3216T=
XM_011516881.1:c.71+3216T=	XP_011515183.1:n.71+3216T=
XR_928569.1:n.1020+34001A=
XR_928570.1:n.1021-20828A=
NM_001172815.2:c.-107+3216T=	NP_001166286.1:n.-107+3216T=
XM_024447083.1:c.-106-8205T=	XP_024302851.1:n.-106-8205T=
XR_928569.2:n.973+34001A=
XR_928570.2:n.974-20828A=
NM_001172811.2:c.-106-8205T=	NP_001166282.1:n.-106-8205T=
NM_001172813.2:c.-107+3216T=	NP_001166284.1:n.-107+3216T=
NM_001172814.2:c.-107+3216T=	NP_001166285.1:n.-107+3216T=
NM_173851.3:c.71+3216T= MANE Select	NP_776250.2:n.71+3216T=
NM_001172815.3:c.-107+3216T=	NP_001166286.1:n.-107+3216T=