Canonical Allele Identifier: CA1813618157

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117077355_117077356delinsAT , CM000670.2:g.117077355_117077356delinsAT	GRCh38
NC_000008.10:g.118089594_118089595delinsAT , CM000670.1:g.118089594_118089595delinsAT	GRCh37
NC_000008.9:g.118158775_118158776delinsAT	NCBI36
NG_016991.1:g.132083_132084delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427715.2:c.-226+38097_-226+38098delinsAT	ENSP00000407505.2:n.-226+38097_-226+38098delinsAT
ENST00000521035.5:n.295-57877_295-57876delinsAT
ENST00000521243.5:c.-106-69464_-106-69463delinsAT	ENSP00000428545.1:n.-106-69464_-106-69463delinsAT
ENST00000524274.5:c.-106-69464_-106-69463delinsAT	ENSP00000427760.1:n.-106-69464_-106-69463delinsAT
NM_001172811.1:c.-106-69464_-106-69463delinsAT	NP_001166282.1:n.-106-69464_-106-69463delinsAT
NM_001172813.1:c.-273-57877_-273-57876delinsAT	NP_001166284.1:n.-273-57877_-273-57876delinsAT
NM_001172815.1:c.-226+38097_-226+38098delinsAT	NP_001166286.1:n.-226+38097_-226+38098delinsAT
XM_011516881.1:c.-96-57877_-96-57876delinsAT	XP_011515183.1:n.-96-57877_-96-57876delinsAT
NM_001172815.2:c.-226+38097_-226+38098delinsAT	NP_001166286.1:n.-226+38097_-226+38098delinsAT
XM_024447083.1:c.-106-69464_-106-69463delinsAT	XP_024302851.1:n.-106-69464_-106-69463delinsAT
NM_001172811.2:c.-106-69464_-106-69463delinsAT	NP_001166282.1:n.-106-69464_-106-69463delinsAT
NM_001172813.2:c.-273-57877_-273-57876delinsAT	NP_001166284.1:n.-273-57877_-273-57876delinsAT
NM_001172815.3:c.-226+38097_-226+38098delinsAT	NP_001166286.1:n.-226+38097_-226+38098delinsAT