Canonical Allele Identifier: CA2695530897
Gene: SLC2A1 HGNC NCBI

Linked Data

dbSNP Id: rs368832648

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927835A>C , CM000663.2:g.42927835A>C GRCh38
NC_000001.10:g.43393506A>C , CM000663.1:g.43393506A>C GRCh37
NC_000001.9:g.43166093A>C NCBI36
NG_008232.1:g.36342T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1075-27T>G MANE Select ENSP00000416293.2:n.1075-27T>G
ENST00000674545.1:n.1665T>G
ENST00000674765.1:c.1030-978T>G ENSP00000501811.1:n.1030-978T>G
ENST00000675112.1:n.1376-27T>G
ENST00000676254.1:n.1524-27T>G
ENST00000426263.7:c.1075-27T>G ENSP00000416293.2:n.1075-27T>G
ENST00000475162.3:c.416-857T>G
ENST00000630287.2:c.*390-27T>G ENSP00000486694.1:n.*390-27T>G
NM_006516.2:c.1075-27T>G NP_006507.2:n.1075-27T>G
NM_006516.3:c.1075-27T>G NP_006507.2:n.1075-27T>G
NM_006516.4:c.1075-27T>G MANE Select NP_006507.2:n.1075-27T>G