Canonical Allele Identifier: CA2772612975
Gene: SLC16A10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111223035A>G , CM000668.2:g.111223035A>G GRCh38
NC_000006.11:g.111544238A>G , CM000668.1:g.111544238A>G GRCh37
NC_000006.10:g.111650931A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*800A>G MANE Select ENSP00000357844.4:n.*800A>G
ENST00000368850.4:c.*800A>G ENSP00000357843.1:n.*800A>G
NM_018593.4:c.*800A>G NP_061063.2:n.*800A>G
XM_017010237.1:c.*800A>G XP_016865726.1:n.*800A>G
XR_001743158.1:n.2630A>G
NM_018593.5:c.*800A>G MANE Select NP_061063.2:n.*800A>G