Canonical Allele Identifier: CA1654828632
Gene: SLC16A10 HGNC NCBI

Linked Data

dbSNP Id: rs1770932730

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222997G>A , CM000668.2:g.111222997G>A GRCh38
NC_000006.11:g.111544200G>A , CM000668.1:g.111544200G>A GRCh37
NC_000006.10:g.111650893G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*762G>A MANE Select ENSP00000357844.4:n.*762G>A
ENST00000368850.4:c.*762G>A ENSP00000357843.1:n.*762G>A
ENST00000368851.9:c.*762G>A ENSP00000357844.4:n.*762G>A
NM_018593.4:c.*762G>A NP_061063.2:n.*762G>A
XM_005266818.2:c.*716G>A XP_005266875.1:n.*716G>A
XM_017010237.1:c.*762G>A XP_016865726.1:n.*762G>A
XR_001743158.1:n.2592G>A
NM_018593.5:c.*762G>A MANE Select NP_061063.2:n.*762G>A