Canonical Allele Identifier: CA339961073

Gene: SLC2A1

Linked Data

• gnomAD v4: 1-42930786-A-G
• MyVariant Identifiers: chr1:g.43396457A>G (hg19) ; chr1:g.42930786A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930786A>G , CM000663.2:g.42930786A>G	GRCh38
NC_000001.10:g.43396457A>G , CM000663.1:g.43396457A>G	GRCh37
NC_000001.9:g.43169044A>G	NCBI36
NG_008232.1:g.33391T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.356T>C MANE Select	ENSP00000416293.2:p.Phe119Ser
ENST00000674765.1:c.356T>C	ENSP00000501811.1:p.Phe119Ser
ENST00000675112.1:n.379T>C
ENST00000676254.1:n.805T>C
ENST00000372500.4:c.260T>C	ENSP00000361578.4:p.Phe87Ser
ENST00000426263.7:c.356T>C	ENSP00000416293.2:p.Phe119Ser
ENST00000439722.2:c.235T>C	ENSP00000395521.2:n.235T>C
ENST00000475162.3:c.255T>C
ENST00000625233.2:n.564T>C
ENST00000630287.2:c.356T>C	ENSP00000486694.1:p.Phe119Ser
NM_006516.2:c.356T>C	NP_006507.2:p.Phe119Ser
NM_006516.3:c.356T>C	NP_006507.2:p.Phe119Ser
NM_006516.4:c.356T>C MANE Select	NP_006507.2:p.Phe119Ser