Canonical Allele Identifier: CA417543711

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43396363T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930692T>G , CM000663.2:g.42930692T>G	GRCh38
NC_000001.10:g.43396363T>G , CM000663.1:g.43396363T>G	GRCh37
NC_000001.9:g.43168950T>G	NCBI36
NG_008232.1:g.33485A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.450A>C MANE Select	ENSP00000416293.2:p.Thr150=
ENST00000674765.1:c.450A>C	ENSP00000501811.1:p.Thr150=
ENST00000675112.1:n.473A>C
ENST00000676254.1:n.899A>C
ENST00000426263.7:c.450A>C	ENSP00000416293.2:p.Thr150=
ENST00000439722.2:c.329A>C	ENSP00000395521.2:n.329A>C
ENST00000475162.3:c.349A>C
ENST00000625233.2:n.658A>C
ENST00000630287.2:c.450A>C	ENSP00000486694.1:p.Thr150=
NM_006516.2:c.450A>C	NP_006507.2:p.Thr150=
NM_006516.3:c.450A>C	NP_006507.2:p.Thr150=
NM_006516.4:c.450A>C MANE Select	NP_006507.2:p.Thr150=