Canonical Allele Identifier: CA1654828602
Gene: SLC16A10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222932T= , CM000668.2:g.111222932T= GRCh38
NC_000006.11:g.111544135T= , CM000668.1:g.111544135T= GRCh37
NC_000006.10:g.111650828T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*697T= MANE Select ENSP00000357844.4:n.*697T=
ENST00000368850.4:c.*697T= ENSP00000357843.1:n.*697T=
ENST00000368851.9:c.*697T= ENSP00000357844.4:n.*697T=
NM_018593.4:c.*697T= NP_061063.2:n.*697T=
XM_005266818.2:c.*651T= XP_005266875.1:n.*651T=
XM_017010237.1:c.*697T= XP_016865726.1:n.*697T=
XR_001743158.1:n.2527T=
NM_018593.5:c.*697T= MANE Select NP_061063.2:n.*697T=
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