Canonical Allele Identifier: CA1165412165

Gene: SLC2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929199_42929201delinsCAA , CM000663.2:g.42929199_42929201delinsCAA	GRCh38
NC_000001.10:g.43394870_43394872delinsCAA , CM000663.1:g.43394870_43394872delinsCAA	GRCh37
NC_000001.9:g.43167457_43167459delinsCAA	NCBI36
NG_008232.1:g.34976_34978delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.972+9_972+11delinsTTG MANE Select	ENSP00000416293.2:n.972+9_972+11delinsTTG
ENST00000674545.1:n.299_301delinsTTG
ENST00000674765.1:c.972+9_972+11delinsTTG	ENSP00000501811.1:n.972+9_972+11delinsTTG
ENST00000675112.1:n.1273+9_1273+11delinsTTG
ENST00000676254.1:n.1421+9_1421+11delinsTTG
ENST00000426263.7:c.972+9_972+11delinsTTG	ENSP00000416293.2:n.972+9_972+11delinsTTG
ENST00000439722.2:c.851+9_851+11delinsTTG	ENSP00000395521.2:n.851+9_851+11delinsTTG
ENST00000475162.3:c.415+1425_415+1427delinsTTG
ENST00000630287.2:c.*287+9_*287+11delinsTTG	ENSP00000486694.1:n.*287+9_*287+11delinsTTG
NM_006516.2:c.972+9_972+11delinsTTG	NP_006507.2:n.972+9_972+11delinsTTG
NM_006516.3:c.972+9_972+11delinsTTG	NP_006507.2:n.972+9_972+11delinsTTG
NM_006516.4:c.972+9_972+11delinsTTG MANE Select	NP_006507.2:n.972+9_972+11delinsTTG