Canonical Allele Identifier: CA713150262
Gene: SLC30A4 HGNC NCBI

Linked Data

dbSNP Id: rs1375544211
MyVariant Identifiers: chr15:g.45772350del (hg19) chr15:g.45480152del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480152del , CM000677.2:g.45480152del GRCh38
NC_000015.9:g.45772350del , CM000677.1:g.45772350del GRCh37
NC_000015.8:g.43559642del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261867.5:c.*5011del MANE Select ENSP00000261867.3:n.*5011del
ENST00000261867.4:c.*5011del ENSP00000261867.3:n.*5011del
NM_013309.5:c.*5011del NP_037441.2:n.*5011del
NM_013309.6:c.*5011del MANE Select NP_037441.2:n.*5011del
Search 100 bp 5'
Search 100 bp 3'