Canonical Allele Identifier: CA339960792

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43396398A>C (hg19) ; chr1:g.42930727A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930727A>C , CM000663.2:g.42930727A>C	GRCh38
NC_000001.10:g.43396398A>C , CM000663.1:g.43396398A>C	GRCh37
NC_000001.9:g.43168985A>C	NCBI36
NG_008232.1:g.33450T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.415T>G MANE Select	ENSP00000416293.2:p.Phe139Val
ENST00000674765.1:c.415T>G	ENSP00000501811.1:p.Phe139Val
ENST00000675112.1:n.438T>G
ENST00000676254.1:n.864T>G
ENST00000372500.4:c.319T>G	ENSP00000361578.4:p.Phe107Val
ENST00000426263.7:c.415T>G	ENSP00000416293.2:p.Phe139Val
ENST00000439722.2:c.294T>G	ENSP00000395521.2:n.294T>G
ENST00000475162.3:c.314T>G
ENST00000625233.2:n.623T>G
ENST00000630287.2:c.415T>G	ENSP00000486694.1:p.Phe139Val
NM_006516.2:c.415T>G	NP_006507.2:p.Phe139Val
NM_006516.3:c.415T>G	NP_006507.2:p.Phe139Val
NM_006516.4:c.415T>G MANE Select	NP_006507.2:p.Phe139Val