Canonical Allele Identifier: CA339954355

Gene: SLC2A1

Linked Data

• gnomAD v4: 1-42927786-T-A
• MyVariant Identifiers: chr1:g.43393457T>A (hg19) ; chr1:g.42927786T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42927786T>A , CM000663.2:g.42927786T>A	GRCh38
NC_000001.10:g.43393457T>A , CM000663.1:g.43393457T>A	GRCh37
NC_000001.9:g.43166044T>A	NCBI36
NG_008232.1:g.36391A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.1097A>T MANE Select	ENSP00000416293.2:p.Tyr366Phe
ENST00000674545.1:n.1714A>T
ENST00000674765.1:c.1030-929A>T	ENSP00000501811.1:n.1030-929A>T
ENST00000675112.1:n.1398A>T
ENST00000676254.1:n.1546A>T
ENST00000426263.7:c.1097A>T	ENSP00000416293.2:p.Tyr366Phe
ENST00000475162.3:c.416-808A>T
ENST00000630287.2:c.*412A>T	ENSP00000486694.1:n.*412A>T
NM_006516.2:c.1097A>T	NP_006507.2:p.Tyr366Phe
NM_006516.3:c.1097A>T	NP_006507.2:p.Tyr366Phe
NM_006516.4:c.1097A>T MANE Select	NP_006507.2:p.Tyr366Phe