Canonical Allele Identifier: CA339953088
Community Standard Title: NM_006516.4(SLC2A1):c.1373G>C (p.Arg458Pro)
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927147C>G , CM000663.2:g.42927147C>G GRCh38
NC_000001.10:g.43392818C>G , CM000663.1:g.43392818C>G GRCh37
NC_000001.9:g.43165405C>G NCBI36
NG_008232.1:g.37030G>C

Transcript Alleles

HGVS Amino-acid Change
NM_006516.4:c.1373G>C MANE Select NP_006507.2:p.Arg458Pro
ENST00000426263.10:c.1373G>C MANE Select ENSP00000416293.2:p.Arg458Pro
NM_006516.2:c.1373G>C NP_006507.2:p.Arg458Pro
NM_006516.3:c.1373G>C NP_006507.2:p.Arg458Pro
ENST00000426263.7:c.1373G>C ENSP00000416293.2:p.Arg458Pro
ENST00000475162.3:c.416-169G>C
ENST00000630287.2:c.*688G>C ENSP00000486694.1:n.*688G>C
ENST00000674545.1:n.1990G>C
ENST00000674765.1:c.1030-290G>C ENSP00000501811.1:n.1030-290G>C
ENST00000675112.1:n.1674G>C
ENST00000676254.1:n.1822G>C