Canonical Allele Identifier: CA1654828625
Gene: SLC16A10 HGNC NCBI

Linked Data

dbSNP Id: rs1770932489
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222991A>G , CM000668.2:g.111222991A>G GRCh38
NC_000006.11:g.111544194A>G , CM000668.1:g.111544194A>G GRCh37
NC_000006.10:g.111650887A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*756A>G MANE Select ENSP00000357844.4:n.*756A>G
ENST00000368850.4:c.*756A>G ENSP00000357843.1:n.*756A>G
ENST00000368851.9:c.*756A>G ENSP00000357844.4:n.*756A>G
NM_018593.4:c.*756A>G NP_061063.2:n.*756A>G
XM_005266818.2:c.*710A>G XP_005266875.1:n.*710A>G
XM_017010237.1:c.*756A>G XP_016865726.1:n.*756A>G
XR_001743158.1:n.2586A>G
NM_018593.5:c.*756A>G MANE Select NP_061063.2:n.*756A>G
Search 100 bp 5'
Search 100 bp 3'