Canonical Allele Identifier: CA1813588855

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117013406T= , CM000670.2:g.117013406T=	GRCh38
NC_000008.10:g.118025645T= , CM000670.1:g.118025645T=	GRCh37
NC_000008.9:g.118094826T=	NCBI36
NG_016991.1:g.68134T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001172811.1:c.-107+62287T=	NP_001166282.1:n.-107+62287T=
NM_001172811.2:c.-107+62287T=	NP_001166282.1:n.-107+62287T=
NM_001172813.1:c.-274+6293T=	NP_001166284.1:n.-274+6293T=
NM_001172813.2:c.-274+6293T=	NP_001166284.1:n.-274+6293T=
NM_001172815.1:c.-265-25813T=	NP_001166286.1:n.-265-25813T=
NM_001172815.2:c.-265-25813T=	NP_001166286.1:n.-265-25813T=
NM_001172815.3:c.-265-25813T=	NP_001166286.1:n.-265-25813T=
ENST00000427715.2:c.-265-25813T=	ENSP00000407505.2:n.-265-25813T=
ENST00000521035.5:n.294+6293T=
ENST00000521243.5:c.-107+62287T=	ENSP00000428545.1:n.-107+62287T=
ENST00000524274.5:c.-107+62287T=	ENSP00000427760.1:n.-107+62287T=
XM_011516881.1:c.-97+62287T=	XP_011515183.1:n.-97+62287T=
XM_024447083.1:c.-107+62287T=	XP_024302851.1:n.-107+62287T=