Canonical Allele Identifier: CA1654828506
Gene: SLC16A10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222683A= , CM000668.2:g.111222683A= GRCh38
NC_000006.11:g.111543886A= , CM000668.1:g.111543886A= GRCh37
NC_000006.10:g.111650579A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368851.10:c.*448A= MANE Select ENSP00000357844.4:n.*448A=
ENST00000368850.4:c.*448A= ENSP00000357843.1:n.*448A=
ENST00000368851.9:c.*448A= ENSP00000357844.4:n.*448A=
NM_018593.4:c.*448A= NP_061063.2:n.*448A=
XM_005266818.2:c.*402A= XP_005266875.1:n.*402A=
XM_017010237.1:c.*448A= XP_016865726.1:n.*448A=
XR_001743158.1:n.2278A=
NM_018593.5:c.*448A= MANE Select NP_061063.2:n.*448A=