Canonical Allele Identifier: CA2680016506
Gene: SLC16A10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111223035del , CM000668.2:g.111223035del GRCh38
NC_000006.11:g.111544238del , CM000668.1:g.111544238del GRCh37
NC_000006.10:g.111650931del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*800del MANE Select ENSP00000357844.4:n.*800del
ENST00000368850.4:c.*800del ENSP00000357843.1:n.*800del
NM_018593.4:c.*800del NP_061063.2:n.*800del
XM_017010237.1:c.*800del XP_016865726.1:n.*800del
XR_001743158.1:n.2630del
NM_018593.5:c.*800del MANE Select NP_061063.2:n.*800del