Canonical Allele Identifier: CA16042369
Community Standard Title: NM_006516.4(SLC2A1):c.1256G>T (p.Gly419Val)
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927627C>A , CM000663.2:g.42927627C>A GRCh38
NC_000001.10:g.43393298C>A , CM000663.1:g.43393298C>A GRCh37
NC_000001.9:g.43165885C>A NCBI36
NG_008232.1:g.36550G>T

Transcript Alleles

HGVS Amino-acid Change
NM_006516.4:c.1256G>T MANE Select NP_006507.2:p.Gly419Val
ENST00000426263.10:c.1256G>T MANE Select ENSP00000416293.2:p.Gly419Val
NM_006516.2:c.1256G>T NP_006507.2:p.Gly419Val
NM_006516.3:c.1256G>T NP_006507.2:p.Gly419Val
ENST00000426263.7:c.1256G>T ENSP00000416293.2:p.Gly419Val
ENST00000475162.3:c.416-649G>T
ENST00000630287.2:c.*571G>T ENSP00000486694.1:n.*571G>T
ENST00000674545.1:n.1873G>T
ENST00000674765.1:c.1030-770G>T ENSP00000501811.1:n.1030-770G>T
ENST00000675112.1:n.1557G>T
ENST00000676254.1:n.1705G>T