Canonical Allele Identifier: CA1654828523
Gene: SLC16A10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222727C= , CM000668.2:g.111222727C= GRCh38
NC_000006.11:g.111543930C= , CM000668.1:g.111543930C= GRCh37
NC_000006.10:g.111650623C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*492C= MANE Select ENSP00000357844.4:n.*492C=
ENST00000368850.4:c.*492C= ENSP00000357843.1:n.*492C=
ENST00000368851.9:c.*492C= ENSP00000357844.4:n.*492C=
NM_018593.4:c.*492C= NP_061063.2:n.*492C=
XM_005266818.2:c.*446C= XP_005266875.1:n.*446C=
XM_017010237.1:c.*492C= XP_016865726.1:n.*492C=
XR_001743158.1:n.2322C=
NM_018593.5:c.*492C= MANE Select NP_061063.2:n.*492C=
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