Canonical Allele Identifier: CA1813618140

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117077313C= , CM000670.2:g.117077313C=	GRCh38
NC_000008.10:g.118089552C= , CM000670.1:g.118089552C=	GRCh37
NC_000008.9:g.118158733C=	NCBI36
NG_016991.1:g.132041C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000427715.2:c.-226+38055C=	ENSP00000407505.2:n.-226+38055C=
ENST00000521035.5:n.295-57919C=
ENST00000521243.5:c.-106-69506C=	ENSP00000428545.1:n.-106-69506C=
ENST00000524274.5:c.-106-69506C=	ENSP00000427760.1:n.-106-69506C=
NM_001172811.1:c.-106-69506C=	NP_001166282.1:n.-106-69506C=
NM_001172813.1:c.-273-57919C=	NP_001166284.1:n.-273-57919C=
NM_001172815.1:c.-226+38055C=	NP_001166286.1:n.-226+38055C=
XM_011516881.1:c.-96-57919C=	XP_011515183.1:n.-96-57919C=
NM_001172815.2:c.-226+38055C=	NP_001166286.1:n.-226+38055C=
XM_024447083.1:c.-106-69506C=	XP_024302851.1:n.-106-69506C=
NM_001172811.2:c.-106-69506C=	NP_001166282.1:n.-106-69506C=
NM_001172813.2:c.-273-57919C=	NP_001166284.1:n.-273-57919C=
NM_001172815.3:c.-226+38055C=	NP_001166286.1:n.-226+38055C=