Canonical Allele Identifier: CA417407573

Gene: SLC2A1

Linked Data

• ClinVar Variation Id: 508424
• ClinVar RCV Id: RCV000601373
• dbSNP Id: rs1553155896
• gnomAD v4: 1-42927788-G-C
• MyVariant Identifiers: chr1:g.43393459G>C (hg19) ; chr1:g.42927788G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42927788G>C , CM000663.2:g.42927788G>C	GRCh38
NC_000001.10:g.43393459G>C , CM000663.1:g.43393459G>C	GRCh37
NC_000001.9:g.43166046G>C	NCBI36
NG_008232.1:g.36389C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.1095C>G MANE Select	ENSP00000416293.2:p.Ser365=
ENST00000674545.1:n.1712C>G
ENST00000674765.1:c.1030-931C>G	ENSP00000501811.1:n.1030-931C>G
ENST00000675112.1:n.1396C>G
ENST00000676254.1:n.1544C>G
ENST00000426263.7:c.1095C>G	ENSP00000416293.2:p.Ser365=
ENST00000475162.3:c.416-810C>G
ENST00000630287.2:c.*410C>G	ENSP00000486694.1:n.*410C>G
NM_006516.2:c.1095C>G	NP_006507.2:p.Ser365=
NM_006516.3:c.1095C>G	NP_006507.2:p.Ser365=
NM_006516.4:c.1095C>G MANE Select	NP_006507.2:p.Ser365=