Canonical Allele Identifier: CA339834819

Gene: MFSD2A

Linked Data

• MyVariant Identifiers: chr1:g.40431177T>A (hg19) ; chr1:g.39965505T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39965505T>A , CM000663.2:g.39965505T>A	GRCh38
NC_000001.10:g.40431177T>A , CM000663.1:g.40431177T>A	GRCh37
NC_000001.9:g.40203764T>A	NCBI36
NG_053084.1:g.15394T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372811.10:c.512T>A MANE Select	ENSP00000361898.6:p.Phe171Tyr
ENST00000372809.5:c.551T>A	ENSP00000361895.5:p.Phe184Tyr
ENST00000372811.9:c.512T>A	ENSP00000361898.5:p.Phe171Tyr
ENST00000420632.6:c.44T>A	ENSP00000391261.2:p.Phe15Tyr
ENST00000434861.5:c.506T>A	ENSP00000407606.1:p.Phe169Tyr
ENST00000469745.5:n.424T>A
ENST00000480630.5:n.1159T>A
ENST00000483824.5:n.647T>A
NM_001136493.2:c.551T>A	NP_001129965.1:p.Phe184Tyr
NM_001287808.1:c.44T>A	NP_001274737.1:p.Phe15Tyr
NM_001287809.1:c.401T>A	NP_001274738.1:p.Phe134Tyr
NM_032793.4:c.512T>A	NP_116182.2:p.Phe171Tyr
NR_109896.1:n.693T>A
XM_005271285.1:c.506T>A	XP_005271342.1:p.Phe169Tyr
XM_011542312.1:c.512T>A	XP_011540614.1:p.Phe171Tyr
XR_946783.1:n.660T>A
NM_001349821.1:c.506T>A	NP_001336750.1:p.Phe169Tyr
NM_001349822.1:c.512T>A	NP_001336751.1:p.Phe171Tyr
NM_001349823.1:c.167T>A	NP_001336752.1:p.Phe56Tyr
NM_001136493.3:c.551T>A	NP_001129965.1:p.Phe184Tyr
NM_001287809.2:c.401T>A	NP_001274738.1:p.Phe134Tyr
NM_001349821.2:c.506T>A	NP_001336750.1:p.Phe169Tyr
NM_001349822.2:c.512T>A	NP_001336751.1:p.Phe171Tyr
NM_001349823.2:c.167T>A	NP_001336752.1:p.Phe56Tyr
NM_032793.5:c.512T>A MANE Select	NP_116182.2:p.Phe171Tyr
NR_109896.2:n.660T>A
NM_001287808.2:c.44T>A	NP_001274737.1:p.Phe15Tyr