Canonical Allele Identifier: CA2680016466
Gene: SLC16A10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222856del , CM000668.2:g.111222856del GRCh38
NC_000006.11:g.111544059del , CM000668.1:g.111544059del GRCh37
NC_000006.10:g.111650752del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*621del MANE Select ENSP00000357844.4:n.*621del
ENST00000368850.4:c.*621del ENSP00000357843.1:n.*621del
ENST00000368851.9:c.*621del ENSP00000357844.4:n.*621del
NM_018593.4:c.*621del NP_061063.2:n.*621del
XM_005266818.2:c.*575del XP_005266875.1:n.*575del
XM_017010237.1:c.*621del XP_016865726.1:n.*621del
XR_001743158.1:n.2451del
NM_018593.5:c.*621del MANE Select NP_061063.2:n.*621del