Canonical Allele Identifier: CA315754762

Gene: SLC2A10

Linked Data

• dbSNP Id: rs564658059
• gnomAD v2: 20-45353478-G-T
• gnomAD v3: 20-46724839-G-T
• gnomAD v4: 20-46724839-G-T
• MyVariant Identifiers: chr20:g.45353478G>T (hg19) ; chr20:g.46724839G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46724839G>T , CM000682.2:g.46724839G>T	GRCh38
NC_000020.10:g.45353478G>T , CM000682.1:g.45353478G>T	GRCh37
NC_000020.9:g.44786885G>T	NCBI36
NG_016284.1:g.20200G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.5-202G>T MANE Select	ENSP00000352216.2:n.5-202G>T
ENST00000359271.3:c.5-202G>T	ENSP00000352216.2:n.5-202G>T
ENST00000611837.1:n.157-202G>T
NM_030777.3:c.5-202G>T	NP_110404.1:n.5-202G>T
XM_011529060.1:c.68-202G>T	XP_011527362.1:n.68-202G>T
XM_011529061.1:c.14-202G>T	XP_011527363.1:n.14-202G>T
XM_011529062.1:c.68-202G>T	XP_011527364.1:n.68-202G>T
XM_011529063.1:c.68-202G>T	XP_011527365.1:n.68-202G>T
XM_011529064.1:c.68-202G>T	XP_011527366.1:n.68-202G>T
XM_011529065.1:c.68-202G>T	XP_011527367.1:n.68-202G>T
XR_936641.1:n.204-202G>T
XM_011529060.2:c.68-202G>T	XP_011527362.1:n.68-202G>T
XM_011529061.2:c.14-202G>T	XP_011527363.1:n.14-202G>T
XM_011529062.2:c.68-202G>T	XP_011527364.1:n.68-202G>T
XM_011529063.2:c.68-202G>T	XP_011527365.1:n.68-202G>T
XM_011529064.2:c.68-202G>T	XP_011527366.1:n.68-202G>T
XM_011529065.2:c.68-202G>T	XP_011527367.1:n.68-202G>T
XM_017028087.2:c.5-202G>T	XP_016883576.1:n.5-202G>T
XR_936641.2:n.191-202G>T
NM_030777.4:c.5-202G>T MANE Select	NP_110404.1:n.5-202G>T