Canonical Allele Identifier: CA145250667
Gene: SLC16A10 HGNC NCBI

Linked Data

dbSNP Id: rs998834870
MyVariant Identifiers: chr6:g.111543837T>C (hg19) chr6:g.111222634T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222634T>C , CM000668.2:g.111222634T>C GRCh38
NC_000006.11:g.111543837T>C , CM000668.1:g.111543837T>C GRCh37
NC_000006.10:g.111650530T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*399T>C MANE Select ENSP00000357844.4:n.*399T>C
ENST00000368850.4:c.*399T>C ENSP00000357843.1:n.*399T>C
ENST00000368851.9:c.*399T>C ENSP00000357844.4:n.*399T>C
NM_018593.4:c.*399T>C NP_061063.2:n.*399T>C
XM_005266818.2:c.*353T>C XP_005266875.1:n.*353T>C
XM_017010237.1:c.*399T>C XP_016865726.1:n.*399T>C
XR_001743158.1:n.2229T>C
NM_018593.5:c.*399T>C MANE Select NP_061063.2:n.*399T>C
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