Canonical Allele Identifier: CA2680016376
Gene: SLC16A10 HGNC NCBI

Linked Data

gnomAD v4: 6-111222687-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222687C>T , CM000668.2:g.111222687C>T GRCh38
NC_000006.11:g.111543890C>T , CM000668.1:g.111543890C>T GRCh37
NC_000006.10:g.111650583C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368851.10:c.*452C>T MANE Select ENSP00000357844.4:n.*452C>T
ENST00000368850.4:c.*452C>T ENSP00000357843.1:n.*452C>T
ENST00000368851.9:c.*452C>T ENSP00000357844.4:n.*452C>T
NM_018593.4:c.*452C>T NP_061063.2:n.*452C>T
XM_005266818.2:c.*406C>T XP_005266875.1:n.*406C>T
XM_017010237.1:c.*452C>T XP_016865726.1:n.*452C>T
XR_001743158.1:n.2282C>T
NM_018593.5:c.*452C>T MANE Select NP_061063.2:n.*452C>T
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