Canonical Allele Identifier: CA1654828635
Gene: SLC16A10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111223018A= , CM000668.2:g.111223018A= GRCh38
NC_000006.11:g.111544221A= , CM000668.1:g.111544221A= GRCh37
NC_000006.10:g.111650914A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*783A= MANE Select ENSP00000357844.4:n.*783A=
ENST00000368850.4:c.*783A= ENSP00000357843.1:n.*783A=
ENST00000368851.9:c.*783A= ENSP00000357844.4:n.*783A=
NM_018593.4:c.*783A= NP_061063.2:n.*783A=
XM_005266818.2:c.*737A= XP_005266875.1:n.*737A=
XM_017010237.1:c.*783A= XP_016865726.1:n.*783A=
XR_001743158.1:n.2613A=
NM_018593.5:c.*783A= MANE Select NP_061063.2:n.*783A=
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