Canonical Allele Identifier: CA1165412090

Gene: SLC2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929041_42929043delinsCAG , CM000663.2:g.42929041_42929043delinsCAG	GRCh38
NC_000001.10:g.43394712_43394714delinsCAG , CM000663.1:g.43394712_43394714delinsCAG	GRCh37
NC_000001.9:g.43167299_43167301delinsCAG	NCBI36
NG_008232.1:g.35134_35136delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.973-10_973-8delinsCTG MANE Select	ENSP00000416293.2:n.973-10_973-8delinsCTG
ENST00000674545.1:n.457_459delinsCTG
ENST00000674765.1:c.973-10_973-8delinsCTG	ENSP00000501811.1:n.973-10_973-8delinsCTG
ENST00000675112.1:n.1274-10_1274-8delinsCTG
ENST00000676254.1:n.1422-10_1422-8delinsCTG
ENST00000426263.7:c.973-10_973-8delinsCTG	ENSP00000416293.2:n.973-10_973-8delinsCTG
ENST00000439722.2:c.852-10_852-8delinsCTG	ENSP00000395521.2:n.852-10_852-8delinsCTG
ENST00000475162.3:c.415+1583_415+1585delinsCTG
ENST00000630287.2:c.*288-10_*288-8delinsCTG	ENSP00000486694.1:n.*288-10_*288-8delinsCTG
NM_006516.2:c.973-10_973-8delinsCTG	NP_006507.2:n.973-10_973-8delinsCTG
NM_006516.3:c.973-10_973-8delinsCTG	NP_006507.2:n.973-10_973-8delinsCTG
NM_006516.4:c.973-10_973-8delinsCTG MANE Select	NP_006507.2:n.973-10_973-8delinsCTG