Canonical Allele Identifier: CA2680016491
Gene: SLC16A10 HGNC NCBI

Linked Data

gnomAD v4: 6-111222933-GC-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222934del , CM000668.2:g.111222934del GRCh38
NC_000006.11:g.111544137del , CM000668.1:g.111544137del GRCh37
NC_000006.10:g.111650830del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*699del MANE Select ENSP00000357844.4:n.*699del
ENST00000368850.4:c.*699del ENSP00000357843.1:n.*699del
ENST00000368851.9:c.*699del ENSP00000357844.4:n.*699del
NM_018593.4:c.*699del NP_061063.2:n.*699del
XM_005266818.2:c.*653del XP_005266875.1:n.*653del
XM_017010237.1:c.*699del XP_016865726.1:n.*699del
XR_001743158.1:n.2529del
NM_018593.5:c.*699del MANE Select NP_061063.2:n.*699del
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Search 100 bp 3'