Canonical Allele Identifier: CA417529515

Gene: MFSD2A

Linked Data

• gnomAD v4: 1-39965521-G-A
• MyVariant Identifiers: chr1:g.40431193G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39965521G>A , CM000663.2:g.39965521G>A	GRCh38
NC_000001.10:g.40431193G>A , CM000663.1:g.40431193G>A	GRCh37
NC_000001.9:g.40203780G>A	NCBI36
NG_053084.1:g.15410G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372811.10:c.528G>A MANE Select	ENSP00000361898.6:p.Gln176=
ENST00000372809.5:c.567G>A	ENSP00000361895.5:p.Gln189=
ENST00000372811.9:c.528G>A	ENSP00000361898.5:p.Gln176=
ENST00000420632.6:c.60G>A	ENSP00000391261.2:p.Gln20=
ENST00000434861.5:c.522G>A	ENSP00000407606.1:p.Gln174=
ENST00000469745.5:n.440G>A
ENST00000480630.5:n.1175G>A
ENST00000483824.5:n.663G>A
NM_001136493.2:c.567G>A	NP_001129965.1:p.Gln189=
NM_001287808.1:c.60G>A	NP_001274737.1:p.Gln20=
NM_001287809.1:c.417G>A	NP_001274738.1:p.Gln139=
NM_032793.4:c.528G>A	NP_116182.2:p.Gln176=
NR_109896.1:n.709G>A
XM_005271285.1:c.522G>A	XP_005271342.1:p.Gln174=
XM_011542312.1:c.528G>A	XP_011540614.1:p.Gln176=
XR_946783.1:n.676G>A
NM_001349821.1:c.522G>A	NP_001336750.1:p.Gln174=
NM_001349822.1:c.528G>A	NP_001336751.1:p.Gln176=
NM_001349823.1:c.183G>A	NP_001336752.1:p.Gln61=
NM_001136493.3:c.567G>A	NP_001129965.1:p.Gln189=
NM_001287809.2:c.417G>A	NP_001274738.1:p.Gln139=
NM_001349821.2:c.522G>A	NP_001336750.1:p.Gln174=
NM_001349822.2:c.528G>A	NP_001336751.1:p.Gln176=
NM_001349823.2:c.183G>A	NP_001336752.1:p.Gln61=
NM_032793.5:c.528G>A MANE Select	NP_116182.2:p.Gln176=
NR_109896.2:n.676G>A
NM_001287808.2:c.60G>A	NP_001274737.1:p.Gln20=