Canonical Allele Identifier: CA510847475
Gene: SLC2A10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.45353900G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725261G>A , CM000682.2:g.46725261G>A GRCh38
NC_000020.10:g.45353900G>A , CM000682.1:g.45353900G>A GRCh37
NC_000020.9:g.44787307G>A NCBI36
NG_016284.1:g.20622G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.225G>A MANE Select ENSP00000352216.2:p.Lys75=
ENST00000359271.3:c.225G>A ENSP00000352216.2:p.Lys75=
ENST00000611837.1:n.377G>A
NM_030777.3:c.225G>A NP_110404.1:p.Lys75=
XM_011529060.1:c.288G>A XP_011527362.1:p.Lys96=
XM_011529061.1:c.234G>A XP_011527363.1:p.Lys78=
XM_011529062.1:c.288G>A XP_011527364.1:p.Lys96=
XM_011529063.1:c.288G>A XP_011527365.1:p.Lys96=
XM_011529064.1:c.288G>A XP_011527366.1:p.Lys96=
XM_011529065.1:c.288G>A XP_011527367.1:p.Lys96=
XR_936641.1:n.424G>A
XM_011529060.2:c.288G>A XP_011527362.1:p.Lys96=
XM_011529061.2:c.234G>A XP_011527363.1:p.Lys78=
XM_011529062.2:c.288G>A XP_011527364.1:p.Lys96=
XM_011529063.2:c.288G>A XP_011527365.1:p.Lys96=
XM_011529064.2:c.288G>A XP_011527366.1:p.Lys96=
XM_011529065.2:c.288G>A XP_011527367.1:p.Lys96=
XM_017028087.2:c.225G>A XP_016883576.1:p.Lys75=
XR_936641.2:n.411G>A
NM_030777.4:c.225G>A MANE Select NP_110404.1:p.Lys75=