Canonical Allele Identifier: CA293543
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 139169
dbSNP Id: rs201323237

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725273C>T , CM000682.2:g.46725273C>T GRCh38
NC_000020.10:g.45353912C>T , CM000682.1:g.45353912C>T GRCh37
NC_000020.9:g.44787319C>T NCBI36
NG_016284.1:g.20634C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000359271.4:c.237C>T MANE Select ENSP00000352216.2:p.Leu79=
ENST00000359271.3:c.237C>T ENSP00000352216.2:p.Leu79=
ENST00000611837.1:n.389C>T
NM_030777.3:c.237C>T NP_110404.1:p.Leu79=
XM_011529060.1:c.300C>T XP_011527362.1:p.Leu100=
XM_011529061.1:c.246C>T XP_011527363.1:p.Leu82=
XM_011529062.1:c.300C>T XP_011527364.1:p.Leu100=
XM_011529063.1:c.300C>T XP_011527365.1:p.Leu100=
XM_011529064.1:c.300C>T XP_011527366.1:p.Leu100=
XM_011529065.1:c.300C>T XP_011527367.1:p.Leu100=
XR_936641.1:n.436C>T
XM_011529060.2:c.300C>T XP_011527362.1:p.Leu100=
XM_011529061.2:c.246C>T XP_011527363.1:p.Leu82=
XM_011529062.2:c.300C>T XP_011527364.1:p.Leu100=
XM_011529063.2:c.300C>T XP_011527365.1:p.Leu100=
XM_011529064.2:c.300C>T XP_011527366.1:p.Leu100=
XM_011529065.2:c.300C>T XP_011527367.1:p.Leu100=
XM_017028087.2:c.237C>T XP_016883576.1:p.Leu79=
XR_936641.2:n.423C>T
NM_030777.4:c.237C>T MANE Select NP_110404.1:p.Leu79=