Canonical Allele Identifier: CA339834630

Gene: MFSD2A

Linked Data

• MyVariant Identifiers: chr1:g.40431144G>T (hg19) ; chr1:g.39965472G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39965472G>T , CM000663.2:g.39965472G>T	GRCh38
NC_000001.10:g.40431144G>T , CM000663.1:g.40431144G>T	GRCh37
NC_000001.9:g.40203731G>T	NCBI36
NG_053084.1:g.15361G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372811.10:c.479G>T MANE Select	ENSP00000361898.6:p.Cys160Phe
ENST00000372809.5:c.518G>T	ENSP00000361895.5:p.Cys173Phe
ENST00000372811.9:c.479G>T	ENSP00000361898.5:p.Cys160Phe
ENST00000420632.6:c.11G>T	ENSP00000391261.2:p.Cys4Phe
ENST00000434861.5:c.473G>T	ENSP00000407606.1:p.Cys158Phe
ENST00000469745.5:n.391G>T
ENST00000480630.5:n.1126G>T
ENST00000483824.5:n.614G>T
NM_001136493.2:c.518G>T	NP_001129965.1:p.Cys173Phe
NM_001287808.1:c.11G>T	NP_001274737.1:p.Cys4Phe
NM_001287809.1:c.368G>T	NP_001274738.1:p.Cys123Phe
NM_032793.4:c.479G>T	NP_116182.2:p.Cys160Phe
NR_109896.1:n.660G>T
XM_005271285.1:c.473G>T	XP_005271342.1:p.Cys158Phe
XM_011542312.1:c.479G>T	XP_011540614.1:p.Cys160Phe
XR_946783.1:n.627G>T
NM_001349821.1:c.473G>T	NP_001336750.1:p.Cys158Phe
NM_001349822.1:c.479G>T	NP_001336751.1:p.Cys160Phe
NM_001349823.1:c.134G>T	NP_001336752.1:p.Cys45Phe
NM_001136493.3:c.518G>T	NP_001129965.1:p.Cys173Phe
NM_001287809.2:c.368G>T	NP_001274738.1:p.Cys123Phe
NM_001349821.2:c.473G>T	NP_001336750.1:p.Cys158Phe
NM_001349822.2:c.479G>T	NP_001336751.1:p.Cys160Phe
NM_001349823.2:c.134G>T	NP_001336752.1:p.Cys45Phe
NM_032793.5:c.479G>T MANE Select	NP_116182.2:p.Cys160Phe
NR_109896.2:n.627G>T
NM_001287808.2:c.11G>T	NP_001274737.1:p.Cys4Phe