Canonical Allele Identifier: CA417409330
Gene: SLC2A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.43395312G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929641G>C , CM000663.2:g.42929641G>C GRCh38
NC_000001.10:g.43395312G>C , CM000663.1:g.43395312G>C GRCh37
NC_000001.9:g.43167899G>C NCBI36
NG_008232.1:g.34536C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.819C>G MANE Select ENSP00000416293.2:p.Leu273=
ENST00000669445.1:c.149C>G
ENST00000674765.1:c.819C>G ENSP00000501811.1:p.Leu273=
ENST00000675112.1:n.842C>G
ENST00000676254.1:n.1268C>G
ENST00000426263.7:c.819C>G ENSP00000416293.2:p.Leu273=
ENST00000439722.2:c.698C>G ENSP00000395521.2:n.698C>G
ENST00000475162.3:c.415+985C>G
ENST00000630287.2:c.*134C>G ENSP00000486694.1:n.*134C>G
NM_006516.2:c.819C>G NP_006507.2:p.Leu273=
NM_006516.3:c.819C>G NP_006507.2:p.Leu273=
NM_006516.4:c.819C>G MANE Select NP_006507.2:p.Leu273=