Canonical Allele Identifier: CA2695703002
Gene: SLC2A1 HGNC NCBI

Linked Data

dbSNP Id: rs2124446613

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927811_42927812insC , CM000663.2:g.42927811_42927812insC GRCh38
NC_000001.10:g.43393482_43393483insC , CM000663.1:g.43393482_43393483insC GRCh37
NC_000001.9:g.43166069_43166070insC NCBI36
NG_008232.1:g.36365_36366insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1075-4_1075-3insG MANE Select ENSP00000416293.2:n.1075-4_1075-3insG
ENST00000674545.1:n.1688_1689insG
ENST00000674765.1:c.1030-955_1030-954insG ENSP00000501811.1:n.1030-955_1030-954insG
ENST00000675112.1:n.1376-4_1376-3insG
ENST00000676254.1:n.1524-4_1524-3insG
ENST00000426263.7:c.1075-4_1075-3insG ENSP00000416293.2:n.1075-4_1075-3insG
ENST00000475162.3:c.416-834_416-833insG
ENST00000630287.2:c.*390-4_*390-3insG ENSP00000486694.1:n.*390-4_*390-3insG
NM_006516.2:c.1075-4_1075-3insG NP_006507.2:n.1075-4_1075-3insG
NM_006516.3:c.1075-4_1075-3insG NP_006507.2:n.1075-4_1075-3insG
NM_006516.4:c.1075-4_1075-3insG MANE Select NP_006507.2:n.1075-4_1075-3insG