Canonical Allele Identifier: CA1654828634
Gene: SLC16A10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111223017G= , CM000668.2:g.111223017G= GRCh38
NC_000006.11:g.111544220G= , CM000668.1:g.111544220G= GRCh37
NC_000006.10:g.111650913G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*782G= MANE Select ENSP00000357844.4:n.*782G=
ENST00000368850.4:c.*782G= ENSP00000357843.1:n.*782G=
ENST00000368851.9:c.*782G= ENSP00000357844.4:n.*782G=
NM_018593.4:c.*782G= NP_061063.2:n.*782G=
XM_005266818.2:c.*736G= XP_005266875.1:n.*736G=
XM_017010237.1:c.*782G= XP_016865726.1:n.*782G=
XR_001743158.1:n.2612G=
NM_018593.5:c.*782G= MANE Select NP_061063.2:n.*782G=
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