Canonical Allele Identifier: CA417543388

Gene: SLC2A1

Linked Data

• gnomAD v4: 1-42929671-G-A
• MyVariant Identifiers: chr1:g.43395342G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929671G>A , CM000663.2:g.42929671G>A	GRCh38
NC_000001.10:g.43395342G>A , CM000663.1:g.43395342G>A	GRCh37
NC_000001.9:g.43167929G>A	NCBI36
NG_008232.1:g.34506C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.789C>T MANE Select	ENSP00000416293.2:p.Phe263=
ENST00000669445.1:c.119C>T
ENST00000674765.1:c.789C>T	ENSP00000501811.1:p.Phe263=
ENST00000675112.1:n.812C>T
ENST00000676254.1:n.1238C>T
ENST00000426263.7:c.789C>T	ENSP00000416293.2:p.Phe263=
ENST00000439722.2:c.668C>T	ENSP00000395521.2:n.668C>T
ENST00000475162.3:c.415+955C>T
ENST00000630287.2:c.*104C>T	ENSP00000486694.1:n.*104C>T
NM_006516.2:c.789C>T	NP_006507.2:p.Phe263=
NM_006516.3:c.789C>T	NP_006507.2:p.Phe263=
NM_006516.4:c.789C>T MANE Select	NP_006507.2:p.Phe263=