Canonical Allele Identifier: CA2680016462
Gene: SLC16A10 HGNC NCBI

Linked Data

gnomAD v4: 6-111222843-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222843A>T , CM000668.2:g.111222843A>T GRCh38
NC_000006.11:g.111544046A>T , CM000668.1:g.111544046A>T GRCh37
NC_000006.10:g.111650739A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*608A>T MANE Select ENSP00000357844.4:n.*608A>T
ENST00000368850.4:c.*608A>T ENSP00000357843.1:n.*608A>T
ENST00000368851.9:c.*608A>T ENSP00000357844.4:n.*608A>T
NM_018593.4:c.*608A>T NP_061063.2:n.*608A>T
XM_005266818.2:c.*562A>T XP_005266875.1:n.*562A>T
XM_017010237.1:c.*608A>T XP_016865726.1:n.*608A>T
XR_001743158.1:n.2438A>T
NM_018593.5:c.*608A>T MANE Select NP_061063.2:n.*608A>T
Search 100 bp 5'
Search 100 bp 3'