Canonical Allele Identifier: CA145250774
Gene: SLC16A10 HGNC NCBI

Linked Data

dbSNP Id: rs966928882
gnomAD v3: 6-111222945-A-C
gnomAD v4: 6-111222945-A-C
MyVariant Identifiers: chr6:g.111544148A>C (hg19) chr6:g.111222945A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222945A>C , CM000668.2:g.111222945A>C GRCh38
NC_000006.11:g.111544148A>C , CM000668.1:g.111544148A>C GRCh37
NC_000006.10:g.111650841A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*710A>C MANE Select ENSP00000357844.4:n.*710A>C
ENST00000368850.4:c.*710A>C ENSP00000357843.1:n.*710A>C
ENST00000368851.9:c.*710A>C ENSP00000357844.4:n.*710A>C
NM_018593.4:c.*710A>C NP_061063.2:n.*710A>C
XM_005266818.2:c.*664A>C XP_005266875.1:n.*664A>C
XM_017010237.1:c.*710A>C XP_016865726.1:n.*710A>C
XR_001743158.1:n.2540A>C
NM_018593.5:c.*710A>C MANE Select NP_061063.2:n.*710A>C
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