Canonical Allele Identifier: CA817165922
Gene: SLC16A10 HGNC NCBI

Linked Data

dbSNP Id: rs1490193575
gnomAD v3: 6-111222992-A-G
gnomAD v4: 6-111222992-A-G
MyVariant Identifiers: chr6:g.111544195A>G (hg19) chr6:g.111222992A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222992A>G , CM000668.2:g.111222992A>G GRCh38
NC_000006.11:g.111544195A>G , CM000668.1:g.111544195A>G GRCh37
NC_000006.10:g.111650888A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*757A>G MANE Select ENSP00000357844.4:n.*757A>G
ENST00000368850.4:c.*757A>G ENSP00000357843.1:n.*757A>G
ENST00000368851.9:c.*757A>G ENSP00000357844.4:n.*757A>G
NM_018593.4:c.*757A>G NP_061063.2:n.*757A>G
XM_005266818.2:c.*711A>G XP_005266875.1:n.*711A>G
XM_017010237.1:c.*757A>G XP_016865726.1:n.*757A>G
XR_001743158.1:n.2587A>G
NM_018593.5:c.*757A>G MANE Select NP_061063.2:n.*757A>G
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