Canonical Allele Identifier: CA1165412296

Gene: SLC2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929513_42929514delinsCA , CM000663.2:g.42929513_42929514delinsCA	GRCh38
NC_000001.10:g.43395184_43395185delinsCA , CM000663.1:g.43395184_43395185delinsCA	GRCh37
NC_000001.9:g.43167771_43167772delinsCA	NCBI36
NG_008232.1:g.34663_34664delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.867+79_867+80delinsTG MANE Select	ENSP00000416293.2:n.867+79_867+80delinsTG
ENST00000674765.1:c.867+79_867+80delinsTG	ENSP00000501811.1:n.867+79_867+80delinsTG
ENST00000675112.1:n.969_970delinsTG
ENST00000676254.1:n.1316+79_1316+80delinsTG
ENST00000426263.7:c.867+79_867+80delinsTG	ENSP00000416293.2:n.867+79_867+80delinsTG
ENST00000439722.2:c.746+79_746+80delinsTG	ENSP00000395521.2:n.746+79_746+80delinsTG
ENST00000475162.3:c.415+1112_415+1113delinsTG
ENST00000630287.2:c.*182+79_*182+80delinsTG	ENSP00000486694.1:n.*182+79_*182+80delinsTG
NM_006516.2:c.867+79_867+80delinsTG	NP_006507.2:n.867+79_867+80delinsTG
NM_006516.3:c.867+79_867+80delinsTG	NP_006507.2:n.867+79_867+80delinsTG
NM_006516.4:c.867+79_867+80delinsTG MANE Select	NP_006507.2:n.867+79_867+80delinsTG