Canonical Allele Identifier: CA2718349811

Gene: SLC30A8

Linked Data

• dbSNP Id: rs2130806993

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117077400_117077403del , CM000670.2:g.117077400_117077403del	GRCh38
NC_000008.10:g.118089639_118089642del , CM000670.1:g.118089639_118089642del	GRCh37
NC_000008.9:g.118158820_118158823del	NCBI36
NG_016991.1:g.132128_132131del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427715.2:c.-226+38142_-226+38145del	ENSP00000407505.2:n.-226+38142_-226+38145del
ENST00000521035.5:n.295-57832_295-57829del
ENST00000521243.5:c.-106-69419_-106-69416del	ENSP00000428545.1:n.-106-69419_-106-69416del
ENST00000524274.5:c.-106-69419_-106-69416del	ENSP00000427760.1:n.-106-69419_-106-69416del
NM_001172811.1:c.-106-69419_-106-69416del	NP_001166282.1:n.-106-69419_-106-69416del
NM_001172813.1:c.-273-57832_-273-57829del	NP_001166284.1:n.-273-57832_-273-57829del
NM_001172815.1:c.-226+38142_-226+38145del	NP_001166286.1:n.-226+38142_-226+38145del
XM_011516881.1:c.-96-57832_-96-57829del	XP_011515183.1:n.-96-57832_-96-57829del
NM_001172815.2:c.-226+38142_-226+38145del	NP_001166286.1:n.-226+38142_-226+38145del
XM_024447083.1:c.-106-69419_-106-69416del	XP_024302851.1:n.-106-69419_-106-69416del
NM_001172811.2:c.-106-69419_-106-69416del	NP_001166282.1:n.-106-69419_-106-69416del
NM_001172813.2:c.-273-57832_-273-57829del	NP_001166284.1:n.-273-57832_-273-57829del
NM_001172815.3:c.-226+38142_-226+38145del	NP_001166286.1:n.-226+38142_-226+38145del