Canonical Allele Identifier: CA522805084

Gene: SLC2A1

Linked Data

• dbSNP Id: rs1324590299
• gnomAD v2: 1-43395064-C-A
• gnomAD v3: 1-42929393-C-A
• gnomAD v4: 1-42929393-C-A
• MyVariant Identifiers: chr1:g.43395064C>A (hg19) ; chr1:g.42929393C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929393C>A , CM000663.2:g.42929393C>A	GRCh38
NC_000001.10:g.43395064C>A , CM000663.1:g.43395064C>A	GRCh37
NC_000001.9:g.43167651C>A	NCBI36
NG_008232.1:g.34784G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.868-79G>T MANE Select	ENSP00000416293.2:n.868-79G>T
ENST00000674545.1:n.107G>T
ENST00000674765.1:c.868-79G>T	ENSP00000501811.1:n.868-79G>T
ENST00000675112.1:n.1090G>T
ENST00000676254.1:n.1317-79G>T
ENST00000426263.7:c.868-79G>T	ENSP00000416293.2:n.868-79G>T
ENST00000439722.2:c.747-79G>T	ENSP00000395521.2:n.747-79G>T
ENST00000475162.3:c.415+1233G>T
ENST00000630287.2:c.*183-79G>T	ENSP00000486694.1:n.*183-79G>T
NM_006516.2:c.868-79G>T	NP_006507.2:n.868-79G>T
NM_006516.3:c.868-79G>T	NP_006507.2:n.868-79G>T
NM_006516.4:c.868-79G>T MANE Select	NP_006507.2:n.868-79G>T