Canonical Allele Identifier: CA2680016485
Gene: SLC16A10 HGNC NCBI

Linked Data

gnomAD v4: 6-111222918-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222918C>A , CM000668.2:g.111222918C>A GRCh38
NC_000006.11:g.111544121C>A , CM000668.1:g.111544121C>A GRCh37
NC_000006.10:g.111650814C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*683C>A MANE Select ENSP00000357844.4:n.*683C>A
ENST00000368850.4:c.*683C>A ENSP00000357843.1:n.*683C>A
ENST00000368851.9:c.*683C>A ENSP00000357844.4:n.*683C>A
NM_018593.4:c.*683C>A NP_061063.2:n.*683C>A
XM_005266818.2:c.*637C>A XP_005266875.1:n.*637C>A
XM_017010237.1:c.*683C>A XP_016865726.1:n.*683C>A
XR_001743158.1:n.2513C>A
NM_018593.5:c.*683C>A MANE Select NP_061063.2:n.*683C>A
Search 100 bp 5'
Search 100 bp 3'