Canonical Allele Identifier: CA417409353
Gene: SLC2A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.43395333G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929662G>T , CM000663.2:g.42929662G>T GRCh38
NC_000001.10:g.43395333G>T , CM000663.1:g.43395333G>T GRCh37
NC_000001.9:g.43167920G>T NCBI36
NG_008232.1:g.34515C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.798C>A MANE Select ENSP00000416293.2:p.Pro266=
ENST00000669445.1:c.128C>A
ENST00000674765.1:c.798C>A ENSP00000501811.1:p.Pro266=
ENST00000675112.1:n.821C>A
ENST00000676254.1:n.1247C>A
ENST00000426263.7:c.798C>A ENSP00000416293.2:p.Pro266=
ENST00000439722.2:c.677C>A ENSP00000395521.2:n.677C>A
ENST00000475162.3:c.415+964C>A
ENST00000630287.2:c.*113C>A ENSP00000486694.1:n.*113C>A
NM_006516.2:c.798C>A NP_006507.2:p.Pro266=
NM_006516.3:c.798C>A NP_006507.2:p.Pro266=
NM_006516.4:c.798C>A MANE Select NP_006507.2:p.Pro266=