Canonical Allele Identifier: CA9891953

Gene: SLC2A10

Linked Data

• ClinVar Variation Id: 263815
• ClinVar RCV Id: RCV000245478 ; RCV000471356 ; RCV001705390 ; RCV002271481
• dbSNP Id: rs150800734
• ExAC: 20:45353990 C / T
• gnomAD v2: 20-45353990-C-T
• gnomAD v3: 20-46725351-C-T
• gnomAD v4: 20-46725351-C-T
• MyVariant Identifiers: chr20:g.45353990C>T (hg19) ; chr20:g.46725351C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725351C>T , CM000682.2:g.46725351C>T	GRCh38
NC_000020.10:g.45353990C>T , CM000682.1:g.45353990C>T	GRCh37
NC_000020.9:g.44787397C>T	NCBI36
NG_016284.1:g.20712C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.315C>T MANE Select	ENSP00000352216.2:p.Arg105=
ENST00000359271.3:c.315C>T	ENSP00000352216.2:p.Arg105=
ENST00000611837.1:n.467C>T
NM_030777.3:c.315C>T	NP_110404.1:p.Arg105=
XM_011529060.1:c.378C>T	XP_011527362.1:p.Arg126=
XM_011529061.1:c.324C>T	XP_011527363.1:p.Arg108=
XM_011529062.1:c.378C>T	XP_011527364.1:p.Arg126=
XM_011529063.1:c.378C>T	XP_011527365.1:p.Arg126=
XM_011529064.1:c.378C>T	XP_011527366.1:p.Arg126=
XM_011529065.1:c.378C>T	XP_011527367.1:p.Arg126=
XR_936641.1:n.514C>T
XM_011529060.2:c.378C>T	XP_011527362.1:p.Arg126=
XM_011529061.2:c.324C>T	XP_011527363.1:p.Arg108=
XM_011529062.2:c.378C>T	XP_011527364.1:p.Arg126=
XM_011529063.2:c.378C>T	XP_011527365.1:p.Arg126=
XM_011529064.2:c.378C>T	XP_011527366.1:p.Arg126=
XM_011529065.2:c.378C>T	XP_011527367.1:p.Arg126=
XM_017028087.2:c.315C>T	XP_016883576.1:p.Arg105=
XR_936641.2:n.501C>T
NM_030777.4:c.315C>T MANE Select	NP_110404.1:p.Arg105=