Canonical Allele Identifier: CA417412013

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43408954T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42943283T>G , CM000663.2:g.42943283T>G	GRCh38
NC_000001.10:g.43408954T>G , CM000663.1:g.43408954T>G	GRCh37
NC_000001.9:g.43181541T>G	NCBI36
NG_008232.1:g.20894A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.57A>C MANE Select	ENSP00000416293.2:p.Ala19=
ENST00000674765.1:c.57A>C	ENSP00000501811.1:p.Ala19=
ENST00000675112.1:n.80A>C
ENST00000372500.4:c.19-12077A>C	ENSP00000361578.4:n.19-12077A>C
ENST00000415851.6:n.274A>C
ENST00000426263.7:c.57A>C	ENSP00000416293.2:p.Ala19=
ENST00000625233.2:n.265A>C
ENST00000628173.1:n.276A>C
ENST00000630287.2:c.57A>C	ENSP00000486694.1:p.Ala19=
ENST00000630821.1:n.274A>C
NM_006516.2:c.57A>C	NP_006507.2:p.Ala19=
NM_006516.3:c.57A>C	NP_006507.2:p.Ala19=
NM_006516.4:c.57A>C MANE Select	NP_006507.2:p.Ala19=