Canonical Allele Identifier: CA2366796080

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725203_46725204delinsTG , CM000682.2:g.46725203_46725204delinsTG	GRCh38
NC_000020.10:g.45353842_45353843delinsTG , CM000682.1:g.45353842_45353843delinsTG	GRCh37
NC_000020.9:g.44787249_44787250delinsTG	NCBI36
NG_016284.1:g.20564_20565delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.167_168delinsTG MANE Select	ENSP00000352216.2:p.Leu56=
ENST00000359271.3:c.167_168delinsTG	ENSP00000352216.2:p.Leu56=
ENST00000611837.1:n.319_320delinsTG
NM_030777.3:c.167_168delinsTG	NP_110404.1:p.Leu56=
XM_011529060.1:c.230_231delinsTG	XP_011527362.1:p.Leu77=
XM_011529061.1:c.176_177delinsTG	XP_011527363.1:p.Leu59=
XM_011529062.1:c.230_231delinsTG	XP_011527364.1:p.Leu77=
XM_011529063.1:c.230_231delinsTG	XP_011527365.1:p.Leu77=
XM_011529064.1:c.230_231delinsTG	XP_011527366.1:p.Leu77=
XM_011529065.1:c.230_231delinsTG	XP_011527367.1:p.Leu77=
XR_936641.1:n.366_367delinsTG
XM_011529060.2:c.230_231delinsTG	XP_011527362.1:p.Leu77=
XM_011529061.2:c.176_177delinsTG	XP_011527363.1:p.Leu59=
XM_011529062.2:c.230_231delinsTG	XP_011527364.1:p.Leu77=
XM_011529063.2:c.230_231delinsTG	XP_011527365.1:p.Leu77=
XM_011529064.2:c.230_231delinsTG	XP_011527366.1:p.Leu77=
XM_011529065.2:c.230_231delinsTG	XP_011527367.1:p.Leu77=
XM_017028087.2:c.167_168delinsTG	XP_016883576.1:p.Leu56=
XR_936641.2:n.353_354delinsTG
NM_030777.4:c.167_168delinsTG MANE Select	NP_110404.1:p.Leu56=