Canonical Allele Identifier: CA1654828622
Gene: SLC16A10 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222984C= , CM000668.2:g.111222984C= GRCh38
NC_000006.11:g.111544187C= , CM000668.1:g.111544187C= GRCh37
NC_000006.10:g.111650880C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*749C= MANE Select ENSP00000357844.4:n.*749C=
ENST00000368850.4:c.*749C= ENSP00000357843.1:n.*749C=
ENST00000368851.9:c.*749C= ENSP00000357844.4:n.*749C=
NM_018593.4:c.*749C= NP_061063.2:n.*749C=
XM_005266818.2:c.*703C= XP_005266875.1:n.*703C=
XM_017010237.1:c.*749C= XP_016865726.1:n.*749C=
XR_001743158.1:n.2579C=
NM_018593.5:c.*749C= MANE Select NP_061063.2:n.*749C=
Search 100 bp 5'
Search 100 bp 3'