Canonical Allele Identifier: CA339964886

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43408973A>C (hg19) ; chr1:g.42943302A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42943302A>C , CM000663.2:g.42943302A>C	GRCh38
NC_000001.10:g.43408973A>C , CM000663.1:g.43408973A>C	GRCh37
NC_000001.9:g.43181560A>C	NCBI36
NG_008232.1:g.20875T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.38T>G MANE Select	ENSP00000416293.2:p.Met13Arg
ENST00000674765.1:c.38T>G	ENSP00000501811.1:p.Met13Arg
ENST00000675112.1:n.61T>G
ENST00000372500.4:c.19-12096T>G	ENSP00000361578.4:n.19-12096T>G
ENST00000415851.6:n.255T>G
ENST00000426263.7:c.38T>G	ENSP00000416293.2:p.Met13Arg
ENST00000625233.2:n.246T>G
ENST00000628173.1:n.257T>G
ENST00000630287.2:c.38T>G	ENSP00000486694.1:p.Met13Arg
ENST00000630821.1:n.255T>G
NM_006516.2:c.38T>G	NP_006507.2:p.Met13Arg
NM_006516.3:c.38T>G	NP_006507.2:p.Met13Arg
NM_006516.4:c.38T>G MANE Select	NP_006507.2:p.Met13Arg