Canonical Allele Identifier: CA409266416
Gene: SLC2A10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725172G>T , CM000682.2:g.46725172G>T GRCh38
NC_000020.10:g.45353811G>T , CM000682.1:g.45353811G>T GRCh37
NC_000020.9:g.44787218G>T NCBI36
NG_016284.1:g.20533G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.136G>T MANE Select ENSP00000352216.2:p.Glu46Ter
ENST00000359271.3:c.136G>T ENSP00000352216.2:p.Glu46Ter
ENST00000611837.1:n.288G>T
NM_030777.3:c.136G>T NP_110404.1:p.Glu46Ter
XM_011529060.1:c.199G>T XP_011527362.1:p.Glu67Ter
XM_011529061.1:c.145G>T XP_011527363.1:p.Glu49Ter
XM_011529062.1:c.199G>T XP_011527364.1:p.Glu67Ter
XM_011529063.1:c.199G>T XP_011527365.1:p.Glu67Ter
XM_011529064.1:c.199G>T XP_011527366.1:p.Glu67Ter
XM_011529065.1:c.199G>T XP_011527367.1:p.Glu67Ter
XR_936641.1:n.335G>T
XM_011529060.2:c.199G>T XP_011527362.1:p.Glu67Ter
XM_011529061.2:c.145G>T XP_011527363.1:p.Glu49Ter
XM_011529062.2:c.199G>T XP_011527364.1:p.Glu67Ter
XM_011529063.2:c.199G>T XP_011527365.1:p.Glu67Ter
XM_011529064.2:c.199G>T XP_011527366.1:p.Glu67Ter
XM_011529065.2:c.199G>T XP_011527367.1:p.Glu67Ter
XM_017028087.2:c.136G>T XP_016883576.1:p.Glu46Ter
XR_936641.2:n.322G>T
NM_030777.4:c.136G>T MANE Select NP_110404.1:p.Glu46Ter