Canonical Allele Identifier: CA145250749
Gene: SLC16A10 HGNC NCBI

Linked Data

dbSNP Id: rs994679401
gnomAD v3: 6-111222896-T-A
gnomAD v4: 6-111222896-T-A
MyVariant Identifiers: chr6:g.111544099T>A (hg19) chr6:g.111222896T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222896T>A , CM000668.2:g.111222896T>A GRCh38
NC_000006.11:g.111544099T>A , CM000668.1:g.111544099T>A GRCh37
NC_000006.10:g.111650792T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*661T>A MANE Select ENSP00000357844.4:n.*661T>A
ENST00000368850.4:c.*661T>A ENSP00000357843.1:n.*661T>A
ENST00000368851.9:c.*661T>A ENSP00000357844.4:n.*661T>A
NM_018593.4:c.*661T>A NP_061063.2:n.*661T>A
XM_005266818.2:c.*615T>A XP_005266875.1:n.*615T>A
XM_017010237.1:c.*661T>A XP_016865726.1:n.*661T>A
XR_001743158.1:n.2491T>A
NM_018593.5:c.*661T>A MANE Select NP_061063.2:n.*661T>A
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