Canonical Allele Identifier: CA339957697
Community Standard Title: NM_006516.4(SLC2A1):c.789C>A (p.Phe263Leu)
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929671G>T , CM000663.2:g.42929671G>T GRCh38
NC_000001.10:g.43395342G>T , CM000663.1:g.43395342G>T GRCh37
NC_000001.9:g.43167929G>T NCBI36
NG_008232.1:g.34506C>A

Transcript Alleles

HGVS Amino-acid Change
NM_006516.4:c.789C>A MANE Select NP_006507.2:p.Phe263Leu
ENST00000426263.10:c.789C>A MANE Select ENSP00000416293.2:p.Phe263Leu
NM_006516.2:c.789C>A NP_006507.2:p.Phe263Leu
NM_006516.3:c.789C>A NP_006507.2:p.Phe263Leu
ENST00000426263.7:c.789C>A ENSP00000416293.2:p.Phe263Leu
ENST00000439722.2:c.668C>A ENSP00000395521.2:n.668C>A
ENST00000475162.3:c.415+955C>A
ENST00000630287.2:c.*104C>A ENSP00000486694.1:n.*104C>A
ENST00000669445.1:c.119C>A
ENST00000674765.1:c.789C>A ENSP00000501811.1:p.Phe263Leu
ENST00000675112.1:n.812C>A
ENST00000676254.1:n.1238C>A