Canonical Allele Identifier: CA339960955
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930760T>G , CM000663.2:g.42930760T>G GRCh38
NC_000001.10:g.43396431T>G , CM000663.1:g.43396431T>G GRCh37
NC_000001.9:g.43169018T>G NCBI36
NG_008232.1:g.33417A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.382A>C MANE Select ENSP00000416293.2:p.Ile128Leu
ENST00000674765.1:c.382A>C ENSP00000501811.1:p.Ile128Leu
ENST00000675112.1:n.405A>C
ENST00000676254.1:n.831A>C
ENST00000372500.4:c.286A>C ENSP00000361578.4:p.Ile96Leu
ENST00000426263.7:c.382A>C ENSP00000416293.2:p.Ile128Leu
ENST00000439722.2:c.261A>C ENSP00000395521.2:n.261A>C
ENST00000475162.3:c.281A>C
ENST00000625233.2:n.590A>C
ENST00000630287.2:c.382A>C ENSP00000486694.1:p.Ile128Leu
NM_006516.2:c.382A>C NP_006507.2:p.Ile128Leu
NM_006516.3:c.382A>C NP_006507.2:p.Ile128Leu
NM_006516.4:c.382A>C MANE Select NP_006507.2:p.Ile128Leu