Canonical Allele Identifier: CA2680016464
Gene: SLC16A10 HGNC NCBI

Linked Data

gnomAD v4: 6-111222846-TGA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222849_111222850del , CM000668.2:g.111222849_111222850del GRCh38
NC_000006.11:g.111544052_111544053del , CM000668.1:g.111544052_111544053del GRCh37
NC_000006.10:g.111650745_111650746del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*614_*615del MANE Select ENSP00000357844.4:n.*614_*615del
ENST00000368850.4:c.*614_*615del ENSP00000357843.1:n.*614_*615del
ENST00000368851.9:c.*614_*615del ENSP00000357844.4:n.*614_*615del
NM_018593.4:c.*614_*615del NP_061063.2:n.*614_*615del
XM_005266818.2:c.*568_*569del XP_005266875.1:n.*568_*569del
XM_017010237.1:c.*614_*615del XP_016865726.1:n.*614_*615del
XR_001743158.1:n.2444_2445del
NM_018593.5:c.*614_*615del MANE Select NP_061063.2:n.*614_*615del
Search 100 bp 5'
Search 100 bp 3'