Canonical Allele Identifier: CA2680016502
Gene: SLC16A10 HGNC NCBI

Linked Data

gnomAD v4: 6-111222990-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222990C>T , CM000668.2:g.111222990C>T GRCh38
NC_000006.11:g.111544193C>T , CM000668.1:g.111544193C>T GRCh37
NC_000006.10:g.111650886C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*755C>T MANE Select ENSP00000357844.4:n.*755C>T
ENST00000368850.4:c.*755C>T ENSP00000357843.1:n.*755C>T
ENST00000368851.9:c.*755C>T ENSP00000357844.4:n.*755C>T
NM_018593.4:c.*755C>T NP_061063.2:n.*755C>T
XM_005266818.2:c.*709C>T XP_005266875.1:n.*709C>T
XM_017010237.1:c.*755C>T XP_016865726.1:n.*755C>T
XR_001743158.1:n.2585C>T
NM_018593.5:c.*755C>T MANE Select NP_061063.2:n.*755C>T
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