Canonical Allele Identifier: CA9892286
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 338599
dbSNP Id: rs34965637

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46733863C>G , CM000682.2:g.46733863C>G GRCh38
NC_000020.10:g.45362502C>G , CM000682.1:g.45362502C>G GRCh37
NC_000020.9:g.44795909C>G NCBI36
NG_016284.1:g.29224C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000359271.4:c.*29C>G MANE Select ENSP00000352216.2:n.*29C>G
ENST00000359271.3:c.*29C>G ENSP00000352216.2:n.*29C>G
NM_030777.3:c.*29C>G NP_110404.1:n.*29C>G
XM_011529060.1:c.*29C>G XP_011527362.1:n.*29C>G
XM_011529061.1:c.*29C>G XP_011527363.1:n.*29C>G
XM_011529062.1:c.*29C>G XP_011527364.1:n.*29C>G
XM_011529065.1:c.*97C>G XP_011527367.1:n.*97C>G
XR_936641.1:n.1903C>G
XM_011529060.2:c.*29C>G XP_011527362.1:n.*29C>G
XM_011529061.2:c.*29C>G XP_011527363.1:n.*29C>G
XM_011529062.2:c.*29C>G XP_011527364.1:n.*29C>G
XM_011529065.2:c.*97C>G XP_011527367.1:n.*97C>G
XM_017028087.2:c.*97C>G XP_016883576.1:n.*97C>G
XR_936641.2:n.1890C>G
NM_030777.4:c.*29C>G MANE Select NP_110404.1:n.*29C>G