Canonical Allele Identifier: CA1165412575
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930230_42930232delinsAGT , CM000663.2:g.42930230_42930232delinsAGT GRCh38
NC_000001.10:g.43395901_43395903delinsAGT , CM000663.1:g.43395901_43395903delinsAGT GRCh37
NC_000001.9:g.43168488_43168490delinsAGT NCBI36
NG_008232.1:g.33945_33947delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.517-197_517-195delinsACT MANE Select ENSP00000416293.2:n.517-197_517-195delinsACT
ENST00000674765.1:c.517-197_517-195delinsACT ENSP00000501811.1:n.517-197_517-195delinsACT
ENST00000675112.1:n.540-197_540-195delinsACT
ENST00000676254.1:n.966-197_966-195delinsACT
ENST00000426263.7:c.517-197_517-195delinsACT ENSP00000416293.2:n.517-197_517-195delinsACT
ENST00000439722.2:c.396-197_396-195delinsACT ENSP00000395521.2:n.396-197_396-195delinsACT
ENST00000475162.3:c.415+394_415+396delinsACT
ENST00000630287.2:c.516+394_516+396delinsACT ENSP00000486694.1:n.516+394_516+396delinsACT
NM_006516.2:c.517-197_517-195delinsACT NP_006507.2:n.517-197_517-195delinsACT
NM_006516.3:c.517-197_517-195delinsACT NP_006507.2:n.517-197_517-195delinsACT
NM_006516.4:c.517-197_517-195delinsACT MANE Select NP_006507.2:n.517-197_517-195delinsACT