Canonical Allele Identifier: CA409266307
Gene: SLC2A10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725118G>C , CM000682.2:g.46725118G>C GRCh38
NC_000020.10:g.45353757G>C , CM000682.1:g.45353757G>C GRCh37
NC_000020.9:g.44787164G>C NCBI36
NG_016284.1:g.20479G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.82G>C MANE Select ENSP00000352216.2:p.Val28Leu
ENST00000359271.3:c.82G>C ENSP00000352216.2:p.Val28Leu
ENST00000611837.1:n.234G>C
NM_030777.3:c.82G>C NP_110404.1:p.Val28Leu
XM_011529060.1:c.145G>C XP_011527362.1:p.Val49Leu
XM_011529061.1:c.91G>C XP_011527363.1:p.Val31Leu
XM_011529062.1:c.145G>C XP_011527364.1:p.Val49Leu
XM_011529063.1:c.145G>C XP_011527365.1:p.Val49Leu
XM_011529064.1:c.145G>C XP_011527366.1:p.Val49Leu
XM_011529065.1:c.145G>C XP_011527367.1:p.Val49Leu
XR_936641.1:n.281G>C
XM_011529060.2:c.145G>C XP_011527362.1:p.Val49Leu
XM_011529061.2:c.91G>C XP_011527363.1:p.Val31Leu
XM_011529062.2:c.145G>C XP_011527364.1:p.Val49Leu
XM_011529063.2:c.145G>C XP_011527365.1:p.Val49Leu
XM_011529064.2:c.145G>C XP_011527366.1:p.Val49Leu
XM_011529065.2:c.145G>C XP_011527367.1:p.Val49Leu
XM_017028087.2:c.82G>C XP_016883576.1:p.Val28Leu
XR_936641.2:n.268G>C
NM_030777.4:c.82G>C MANE Select NP_110404.1:p.Val28Leu