Canonical Allele Identifier: CA2680016477
Gene: SLC16A10 HGNC NCBI

Linked Data

gnomAD v4: 6-111222902-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222902T>A , CM000668.2:g.111222902T>A GRCh38
NC_000006.11:g.111544105T>A , CM000668.1:g.111544105T>A GRCh37
NC_000006.10:g.111650798T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*667T>A MANE Select ENSP00000357844.4:n.*667T>A
ENST00000368850.4:c.*667T>A ENSP00000357843.1:n.*667T>A
ENST00000368851.9:c.*667T>A ENSP00000357844.4:n.*667T>A
NM_018593.4:c.*667T>A NP_061063.2:n.*667T>A
XM_005266818.2:c.*621T>A XP_005266875.1:n.*621T>A
XM_017010237.1:c.*667T>A XP_016865726.1:n.*667T>A
XR_001743158.1:n.2497T>A
NM_018593.5:c.*667T>A MANE Select NP_061063.2:n.*667T>A
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