Canonical Allele Identifier: CA9891905

Gene: SLC2A10

Linked Data

• ClinVar Variation Id: 513410
• ClinVar RCV Id: RCV000612012
• dbSNP Id: rs772186491
• ExAC: 20:45353729 T / C
• gnomAD v2: 20-45353729-T-C
• gnomAD v4: 20-46725090-T-C
• MyVariant Identifiers: chr20:g.45353729T>C (hg19) ; chr20:g.46725090T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725090T>C , CM000682.2:g.46725090T>C	GRCh38
NC_000020.10:g.45353729T>C , CM000682.1:g.45353729T>C	GRCh37
NC_000020.9:g.44787136T>C	NCBI36
NG_016284.1:g.20451T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.54T>C MANE Select	ENSP00000352216.2:p.Gly18=
ENST00000359271.3:c.54T>C	ENSP00000352216.2:p.Gly18=
ENST00000611837.1:n.206T>C
NM_030777.3:c.54T>C	NP_110404.1:p.Gly18=
XM_011529060.1:c.117T>C	XP_011527362.1:p.Gly39=
XM_011529061.1:c.63T>C	XP_011527363.1:p.Gly21=
XM_011529062.1:c.117T>C	XP_011527364.1:p.Gly39=
XM_011529063.1:c.117T>C	XP_011527365.1:p.Gly39=
XM_011529064.1:c.117T>C	XP_011527366.1:p.Gly39=
XM_011529065.1:c.117T>C	XP_011527367.1:p.Gly39=
XR_936641.1:n.253T>C
XM_011529060.2:c.117T>C	XP_011527362.1:p.Gly39=
XM_011529061.2:c.63T>C	XP_011527363.1:p.Gly21=
XM_011529062.2:c.117T>C	XP_011527364.1:p.Gly39=
XM_011529063.2:c.117T>C	XP_011527365.1:p.Gly39=
XM_011529064.2:c.117T>C	XP_011527366.1:p.Gly39=
XM_011529065.2:c.117T>C	XP_011527367.1:p.Gly39=
XM_017028087.2:c.54T>C	XP_016883576.1:p.Gly18=
XR_936641.2:n.240T>C
NM_030777.4:c.54T>C MANE Select	NP_110404.1:p.Gly18=