Canonical Allele Identifier: CA417543396
Gene: SLC2A1 HGNC NCBI

Linked Data

gnomAD v4: 1-42929682-G-A
MyVariant Identifiers: chr1:g.43395353G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929682G>A , CM000663.2:g.42929682G>A GRCh38
NC_000001.10:g.43395353G>A , CM000663.1:g.43395353G>A GRCh37
NC_000001.9:g.43167940G>A NCBI36
NG_008232.1:g.34495C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.778C>T MANE Select ENSP00000416293.2:p.Leu260=
ENST00000669445.1:c.108C>T
ENST00000674765.1:c.778C>T ENSP00000501811.1:p.Leu260=
ENST00000675112.1:n.801C>T
ENST00000676254.1:n.1227C>T
ENST00000426263.7:c.778C>T ENSP00000416293.2:p.Leu260=
ENST00000439722.2:c.657C>T ENSP00000395521.2:n.657C>T
ENST00000475162.3:c.415+944C>T
ENST00000630287.2:c.*93C>T ENSP00000486694.1:n.*93C>T
NM_006516.2:c.778C>T NP_006507.2:p.Leu260=
NM_006516.3:c.778C>T NP_006507.2:p.Leu260=
NM_006516.4:c.778C>T MANE Select NP_006507.2:p.Leu260=