Canonical Allele Identifier: CA2502065433

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117077252_117077256del , CM000670.2:g.117077252_117077256del	GRCh38
NC_000008.10:g.118089491_118089495del , CM000670.1:g.118089491_118089495del	GRCh37
NC_000008.9:g.118158672_118158676del	NCBI36
NG_016991.1:g.131980_131984del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427715.2:c.-226+37994_-226+37998del	ENSP00000407505.2:n.-226+37994_-226+37998del
ENST00000521035.5:n.295-57980_295-57976del
ENST00000521243.5:c.-106-69567_-106-69563del	ENSP00000428545.1:n.-106-69567_-106-69563del
ENST00000524274.5:c.-106-69567_-106-69563del	ENSP00000427760.1:n.-106-69567_-106-69563del
NM_001172811.1:c.-106-69567_-106-69563del	NP_001166282.1:n.-106-69567_-106-69563del
NM_001172813.1:c.-273-57980_-273-57976del	NP_001166284.1:n.-273-57980_-273-57976del
NM_001172815.1:c.-226+37994_-226+37998del	NP_001166286.1:n.-226+37994_-226+37998del
XM_011516881.1:c.-96-57980_-96-57976del	XP_011515183.1:n.-96-57980_-96-57976del
NM_001172815.2:c.-226+37994_-226+37998del	NP_001166286.1:n.-226+37994_-226+37998del
XM_024447083.1:c.-106-69567_-106-69563del	XP_024302851.1:n.-106-69567_-106-69563del
NM_001172811.2:c.-106-69567_-106-69563del	NP_001166282.1:n.-106-69567_-106-69563del
NM_001172813.2:c.-273-57980_-273-57976del	NP_001166284.1:n.-273-57980_-273-57976del
NM_001172815.3:c.-226+37994_-226+37998del	NP_001166286.1:n.-226+37994_-226+37998del