Canonical Allele Identifier: CA339957440
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929643G>C , CM000663.2:g.42929643G>C GRCh38
NC_000001.10:g.43395314G>C , CM000663.1:g.43395314G>C GRCh37
NC_000001.9:g.43167901G>C NCBI36
NG_008232.1:g.34534C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.817C>G MANE Select ENSP00000416293.2:p.Leu273Val
ENST00000669445.1:c.147C>G
ENST00000674765.1:c.817C>G ENSP00000501811.1:p.Leu273Val
ENST00000675112.1:n.840C>G
ENST00000676254.1:n.1266C>G
ENST00000426263.7:c.817C>G ENSP00000416293.2:p.Leu273Val
ENST00000439722.2:c.696C>G ENSP00000395521.2:n.696C>G
ENST00000475162.3:c.415+983C>G
ENST00000630287.2:c.*132C>G ENSP00000486694.1:n.*132C>G
NM_006516.2:c.817C>G NP_006507.2:p.Leu273Val
NM_006516.3:c.817C>G NP_006507.2:p.Leu273Val
NM_006516.4:c.817C>G MANE Select NP_006507.2:p.Leu273Val