Canonical Allele Identifier: CA1654828562
Gene: SLC16A10 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222826T= , CM000668.2:g.111222826T= GRCh38
NC_000006.11:g.111544029T= , CM000668.1:g.111544029T= GRCh37
NC_000006.10:g.111650722T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*591T= MANE Select ENSP00000357844.4:n.*591T=
ENST00000368850.4:c.*591T= ENSP00000357843.1:n.*591T=
ENST00000368851.9:c.*591T= ENSP00000357844.4:n.*591T=
NM_018593.4:c.*591T= NP_061063.2:n.*591T=
XM_005266818.2:c.*545T= XP_005266875.1:n.*545T=
XM_017010237.1:c.*591T= XP_016865726.1:n.*591T=
XR_001743158.1:n.2421T=
NM_018593.5:c.*591T= MANE Select NP_061063.2:n.*591T=
Search 100 bp 5'
Search 100 bp 3'