Canonical Allele Identifier: CA1813618198

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117077453T= , CM000670.2:g.117077453T=	GRCh38
NC_000008.10:g.118089692T= , CM000670.1:g.118089692T=	GRCh37
NC_000008.9:g.118158873T=	NCBI36
NG_016991.1:g.132181T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427715.2:c.-226+38195T=	ENSP00000407505.2:n.-226+38195T=
ENST00000521035.5:n.295-57779T=
ENST00000521243.5:c.-106-69366T=	ENSP00000428545.1:n.-106-69366T=
ENST00000524274.5:c.-106-69366T=	ENSP00000427760.1:n.-106-69366T=
NM_001172811.1:c.-106-69366T=	NP_001166282.1:n.-106-69366T=
NM_001172813.1:c.-273-57779T=	NP_001166284.1:n.-273-57779T=
NM_001172815.1:c.-226+38195T=	NP_001166286.1:n.-226+38195T=
XM_011516881.1:c.-96-57779T=	XP_011515183.1:n.-96-57779T=
NM_001172815.2:c.-226+38195T=	NP_001166286.1:n.-226+38195T=
XM_024447083.1:c.-106-69366T=	XP_024302851.1:n.-106-69366T=
NM_001172811.2:c.-106-69366T=	NP_001166282.1:n.-106-69366T=
NM_001172813.2:c.-273-57779T=	NP_001166284.1:n.-273-57779T=
NM_001172815.3:c.-226+38195T=	NP_001166286.1:n.-226+38195T=