Canonical Allele Identifier: CA417529523

Gene: MFSD2A

Linked Data

• gnomAD v4: 1-39965528-C-A
• MyVariant Identifiers: chr1:g.40431200C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39965528C>A , CM000663.2:g.39965528C>A	GRCh38
NC_000001.10:g.40431200C>A , CM000663.1:g.40431200C>A	GRCh37
NC_000001.9:g.40203787C>A	NCBI36
NG_053084.1:g.15417C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372811.10:c.535C>A MANE Select	ENSP00000361898.6:p.Arg179=
ENST00000372809.5:c.574C>A	ENSP00000361895.5:p.Arg192=
ENST00000372811.9:c.535C>A	ENSP00000361898.5:p.Arg179=
ENST00000420632.6:c.67C>A	ENSP00000391261.2:p.Arg23=
ENST00000434861.5:c.529C>A	ENSP00000407606.1:p.Arg177=
ENST00000469745.5:n.447C>A
ENST00000480630.5:n.1182C>A
ENST00000483824.5:n.670C>A
NM_001136493.2:c.574C>A	NP_001129965.1:p.Arg192=
NM_001287808.1:c.67C>A	NP_001274737.1:p.Arg23=
NM_001287809.1:c.424C>A	NP_001274738.1:p.Arg142=
NM_032793.4:c.535C>A	NP_116182.2:p.Arg179=
NR_109896.1:n.716C>A
XM_005271285.1:c.529C>A	XP_005271342.1:p.Arg177=
XM_011542312.1:c.535C>A	XP_011540614.1:p.Arg179=
XR_946783.1:n.683C>A
NM_001349821.1:c.529C>A	NP_001336750.1:p.Arg177=
NM_001349822.1:c.535C>A	NP_001336751.1:p.Arg179=
NM_001349823.1:c.190C>A	NP_001336752.1:p.Arg64=
NM_001136493.3:c.574C>A	NP_001129965.1:p.Arg192=
NM_001287809.2:c.424C>A	NP_001274738.1:p.Arg142=
NM_001349821.2:c.529C>A	NP_001336750.1:p.Arg177=
NM_001349822.2:c.535C>A	NP_001336751.1:p.Arg179=
NM_001349823.2:c.190C>A	NP_001336752.1:p.Arg64=
NM_032793.5:c.535C>A MANE Select	NP_116182.2:p.Arg179=
NR_109896.2:n.683C>A
NM_001287808.2:c.67C>A	NP_001274737.1:p.Arg23=