Canonical Allele Identifier: CA2366796020

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725062_46725063delinsCT , CM000682.2:g.46725062_46725063delinsCT	GRCh38
NC_000020.10:g.45353701_45353702delinsCT , CM000682.1:g.45353701_45353702delinsCT	GRCh37
NC_000020.9:g.44787108_44787109delinsCT	NCBI36
NG_016284.1:g.20423_20424delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.26_27delinsCT MANE Select	ENSP00000352216.2:p.Pro9=
ENST00000359271.3:c.26_27delinsCT	ENSP00000352216.2:p.Pro9=
ENST00000611837.1:n.178_179delinsCT
NM_030777.3:c.26_27delinsCT	NP_110404.1:p.Pro9=
XM_011529060.1:c.89_90delinsCT	XP_011527362.1:p.Pro30=
XM_011529061.1:c.35_36delinsCT	XP_011527363.1:p.Pro12=
XM_011529062.1:c.89_90delinsCT	XP_011527364.1:p.Pro30=
XM_011529063.1:c.89_90delinsCT	XP_011527365.1:p.Pro30=
XM_011529064.1:c.89_90delinsCT	XP_011527366.1:p.Pro30=
XM_011529065.1:c.89_90delinsCT	XP_011527367.1:p.Pro30=
XR_936641.1:n.225_226delinsCT
XM_011529060.2:c.89_90delinsCT	XP_011527362.1:p.Pro30=
XM_011529061.2:c.35_36delinsCT	XP_011527363.1:p.Pro12=
XM_011529062.2:c.89_90delinsCT	XP_011527364.1:p.Pro30=
XM_011529063.2:c.89_90delinsCT	XP_011527365.1:p.Pro30=
XM_011529064.2:c.89_90delinsCT	XP_011527366.1:p.Pro30=
XM_011529065.2:c.89_90delinsCT	XP_011527367.1:p.Pro30=
XM_017028087.2:c.26_27delinsCT	XP_016883576.1:p.Pro9=
XR_936641.2:n.212_213delinsCT
NM_030777.4:c.26_27delinsCT MANE Select	NP_110404.1:p.Pro9=