Canonical Allele Identifier: CA2653170692

Gene: SLC2A10

Linked Data

• gnomAD v4: 20-46724935-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46724935G>T , CM000682.2:g.46724935G>T	GRCh38
NC_000020.10:g.45353574G>T , CM000682.1:g.45353574G>T	GRCh37
NC_000020.9:g.44786981G>T	NCBI36
NG_016284.1:g.20296G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.5-106G>T MANE Select	ENSP00000352216.2:n.5-106G>T
ENST00000359271.3:c.5-106G>T	ENSP00000352216.2:n.5-106G>T
ENST00000611837.1:n.157-106G>T
NM_030777.3:c.5-106G>T	NP_110404.1:n.5-106G>T
XM_011529060.1:c.68-106G>T	XP_011527362.1:n.68-106G>T
XM_011529061.1:c.14-106G>T	XP_011527363.1:n.14-106G>T
XM_011529062.1:c.68-106G>T	XP_011527364.1:n.68-106G>T
XM_011529063.1:c.68-106G>T	XP_011527365.1:n.68-106G>T
XM_011529064.1:c.68-106G>T	XP_011527366.1:n.68-106G>T
XM_011529065.1:c.68-106G>T	XP_011527367.1:n.68-106G>T
XR_936641.1:n.204-106G>T
XM_011529060.2:c.68-106G>T	XP_011527362.1:n.68-106G>T
XM_011529061.2:c.14-106G>T	XP_011527363.1:n.14-106G>T
XM_011529062.2:c.68-106G>T	XP_011527364.1:n.68-106G>T
XM_011529063.2:c.68-106G>T	XP_011527365.1:n.68-106G>T
XM_011529064.2:c.68-106G>T	XP_011527366.1:n.68-106G>T
XM_011529065.2:c.68-106G>T	XP_011527367.1:n.68-106G>T
XM_017028087.2:c.5-106G>T	XP_016883576.1:n.5-106G>T
XR_936641.2:n.191-106G>T
NM_030777.4:c.5-106G>T MANE Select	NP_110404.1:n.5-106G>T