Canonical Allele Identifier: CA1813622927

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117138696T= , CM000670.2:g.117138696T=	GRCh38
NC_000008.10:g.118150935T= , CM000670.1:g.118150935T=	GRCh37
NC_000008.9:g.118220116T=	NCBI36
NG_016991.1:g.193424T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.71+3298T= MANE Select	ENSP00000415011.2:n.71+3298T=
ENST00000427715.2:c.-107+3298T=	ENSP00000407505.2:n.-107+3298T=
ENST00000456015.6:c.71+3298T=	ENSP00000415011.2:n.71+3298T=
ENST00000518396.5:c.-107+3298T=	ENSP00000485167.1:n.-107+3298T=
ENST00000518521.5:c.-77+3298T=	ENSP00000485566.1:n.-77+3298T=
ENST00000519688.5:c.-107+3298T=	ENSP00000431069.1:n.-107+3298T=
ENST00000520469.1:n.325+3298T=
ENST00000521035.5:n.461+3298T=
ENST00000521243.5:c.-106-8123T=	ENSP00000428545.1:n.-106-8123T=
ENST00000524274.5:c.-106-8123T=	ENSP00000427760.1:n.-106-8123T=
NM_001172811.1:c.-106-8123T=	NP_001166282.1:n.-106-8123T=
NM_001172813.1:c.-107+3298T=	NP_001166284.1:n.-107+3298T=
NM_001172814.1:c.-107+3298T=	NP_001166285.1:n.-107+3298T=
NM_001172815.1:c.-107+3298T=	NP_001166286.1:n.-107+3298T=
NM_173851.2:c.71+3298T=	NP_776250.2:n.71+3298T=
XM_011516881.1:c.71+3298T=	XP_011515183.1:n.71+3298T=
XR_928569.1:n.1020+33919A=
XR_928570.1:n.1021-20910A=
NM_001172815.2:c.-107+3298T=	NP_001166286.1:n.-107+3298T=
XM_024447083.1:c.-106-8123T=	XP_024302851.1:n.-106-8123T=
XR_928569.2:n.973+33919A=
XR_928570.2:n.974-20910A=
NM_001172811.2:c.-106-8123T=	NP_001166282.1:n.-106-8123T=
NM_001172813.2:c.-107+3298T=	NP_001166284.1:n.-107+3298T=
NM_001172814.2:c.-107+3298T=	NP_001166285.1:n.-107+3298T=
NM_173851.3:c.71+3298T= MANE Select	NP_776250.2:n.71+3298T=
NM_001172815.3:c.-107+3298T=	NP_001166286.1:n.-107+3298T=