Canonical Allele Identifier: CA1140594752

Gene: SLC2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42943231_42943236delinsGGGGGG , CM000663.2:g.42943231_42943236delinsGGGGGG	GRCh38
NC_000001.10:g.43408902_43408907delinsGGGGGG , CM000663.1:g.43408902_43408907delinsGGGGGG	GRCh37
NC_000001.9:g.43181489_43181494delinsGGGGGG	NCBI36
NG_008232.1:g.20941_20946delinsCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.104_109delinsCCCCCC MANE Select	ENSP00000416293.2:p.Ala35=
ENST00000674765.1:c.104_109delinsCCCCCC	ENSP00000501811.1:p.Ala35=
ENST00000675112.1:n.127_132delinsCCCCCC
ENST00000372500.4:c.19-12030_19-12025delinsCCCCCC	ENSP00000361578.4:n.19-12030_19-12025delinsCCCCCC
ENST00000415851.6:n.321_326delinsCCCCCC
ENST00000426263.7:c.104_109delinsCCCCCC	ENSP00000416293.2:p.Ala35=
ENST00000475162.3:c.3_8delinsCCCCCC
ENST00000625233.2:n.312_317delinsCCCCCC
ENST00000628173.1:n.323_328delinsCCCCCC
ENST00000630287.2:c.104_109delinsCCCCCC	ENSP00000486694.1:p.Ala35=
ENST00000630821.1:n.321_326delinsCCCCCC
NM_006516.2:c.104_109delinsCCCCCC	NP_006507.2:p.Ala35=
NM_006516.3:c.104_109delinsCCCCCC	NP_006507.2:p.Ala35=
NM_006516.4:c.104_109delinsCCCCCC MANE Select	NP_006507.2:p.Ala35=