Canonical Allele Identifier: CA1654828547
Gene: SLC16A10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222793T= , CM000668.2:g.111222793T= GRCh38
NC_000006.11:g.111543996T= , CM000668.1:g.111543996T= GRCh37
NC_000006.10:g.111650689T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*558T= MANE Select ENSP00000357844.4:n.*558T=
ENST00000368850.4:c.*558T= ENSP00000357843.1:n.*558T=
ENST00000368851.9:c.*558T= ENSP00000357844.4:n.*558T=
NM_018593.4:c.*558T= NP_061063.2:n.*558T=
XM_005266818.2:c.*512T= XP_005266875.1:n.*512T=
XM_017010237.1:c.*558T= XP_016865726.1:n.*558T=
XR_001743158.1:n.2388T=
NM_018593.5:c.*558T= MANE Select NP_061063.2:n.*558T=
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