Canonical Allele Identifier: CA1001076832

Gene: SLC2A1

Linked Data

• dbSNP Id: rs1387930918
• gnomAD v3: 1-42929385-T-C
• gnomAD v4: 1-42929385-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929385T>C , CM000663.2:g.42929385T>C	GRCh38
NC_000001.10:g.43395056T>C , CM000663.1:g.43395056T>C	GRCh37
NC_000001.9:g.43167643T>C	NCBI36
NG_008232.1:g.34792A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.868-71A>G MANE Select	ENSP00000416293.2:n.868-71A>G
ENST00000674545.1:n.115A>G
ENST00000674765.1:c.868-71A>G	ENSP00000501811.1:n.868-71A>G
ENST00000675112.1:n.1098A>G
ENST00000676254.1:n.1317-71A>G
ENST00000426263.7:c.868-71A>G	ENSP00000416293.2:n.868-71A>G
ENST00000439722.2:c.747-71A>G	ENSP00000395521.2:n.747-71A>G
ENST00000475162.3:c.415+1241A>G
ENST00000630287.2:c.*183-71A>G	ENSP00000486694.1:n.*183-71A>G
NM_006516.2:c.868-71A>G	NP_006507.2:n.868-71A>G
NM_006516.3:c.868-71A>G	NP_006507.2:n.868-71A>G
NM_006516.4:c.868-71A>G MANE Select	NP_006507.2:n.868-71A>G