Canonical Allele Identifier: CA2680016501
Gene: SLC16A10 HGNC NCBI

Linked Data

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

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

Transcript Alleles

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