Canonical Allele Identifier: CA1165417884

Gene: SLC2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42943543_42943545delinsAGG , CM000663.2:g.42943543_42943545delinsAGG	GRCh38
NC_000001.10:g.43409214_43409216delinsAGG , CM000663.1:g.43409214_43409216delinsAGG	GRCh37
NC_000001.9:g.43181801_43181803delinsAGG	NCBI36
NG_008232.1:g.20632_20634delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.19-224_19-222delinsCCT MANE Select	ENSP00000416293.2:n.19-224_19-222delinsCCT
ENST00000674765.1:c.19-224_19-222delinsCCT	ENSP00000501811.1:n.19-224_19-222delinsCCT
ENST00000675112.1:n.42-224_42-222delinsCCT
ENST00000372500.4:c.19-12339_19-12337delinsCCT	ENSP00000361578.4:n.19-12339_19-12337delinsCCT
ENST00000415851.6:n.236-224_236-222delinsCCT
ENST00000426263.7:c.19-224_19-222delinsCCT	ENSP00000416293.2:n.19-224_19-222delinsCCT
ENST00000625233.2:n.227-224_227-222delinsCCT
ENST00000628173.1:n.238-224_238-222delinsCCT
ENST00000630287.2:c.19-224_19-222delinsCCT	ENSP00000486694.1:n.19-224_19-222delinsCCT
ENST00000630821.1:n.236-224_236-222delinsCCT
NM_006516.2:c.19-224_19-222delinsCCT	NP_006507.2:n.19-224_19-222delinsCCT
NM_006516.3:c.19-224_19-222delinsCCT	NP_006507.2:n.19-224_19-222delinsCCT
NM_006516.4:c.19-224_19-222delinsCCT MANE Select	NP_006507.2:n.19-224_19-222delinsCCT