Canonical Allele Identifier: CA9892034

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725782A>G , CM000682.2:g.46725782A>G	GRCh38
NC_000020.10:g.45354421A>G , CM000682.1:g.45354421A>G	GRCh37
NC_000020.9:g.44787828A>G	NCBI36
NG_016284.1:g.21143A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_030777.4:c.746A>G MANE Select	NP_110404.1:p.Asn249Ser
ENST00000359271.4:c.746A>G MANE Select	ENSP00000352216.2:p.Asn249Ser
NM_030777.3:c.746A>G	NP_110404.1:p.Asn249Ser
ENST00000359271.3:c.746A>G	ENSP00000352216.2:p.Asn249Ser
XM_011529060.1:c.809A>G	XP_011527362.1:p.Asn270Ser
XM_011529060.2:c.809A>G	XP_011527362.1:p.Asn270Ser
XM_011529061.1:c.755A>G	XP_011527363.1:p.Asn252Ser
XM_011529061.2:c.755A>G	XP_011527363.1:p.Asn252Ser
XM_011529062.1:c.809A>G	XP_011527364.1:p.Asn270Ser
XM_011529062.2:c.809A>G	XP_011527364.1:p.Asn270Ser
XM_011529063.1:c.809A>G	XP_011527365.1:p.Asn270Ser
XM_011529063.2:c.809A>G	XP_011527365.1:p.Asn270Ser
XM_011529064.1:c.809A>G	XP_011527366.1:p.Asn270Ser
XM_011529064.2:c.809A>G	XP_011527366.1:p.Asn270Ser
XM_011529065.1:c.809A>G	XP_011527367.1:p.Asn270Ser
XM_011529065.2:c.809A>G	XP_011527367.1:p.Asn270Ser
XM_017028087.2:c.746A>G	XP_016883576.1:p.Asn249Ser
XR_936641.1:n.945A>G
XR_936641.2:n.932A>G