Canonical Allele Identifier: CA1164196327

Gene: MFSD2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39965490C= , CM000663.2:g.39965490C=	GRCh38
NC_000001.10:g.40431162C= , CM000663.1:g.40431162C=	GRCh37
NC_000001.9:g.40203749C=	NCBI36
NG_053084.1:g.15379C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372811.10:c.497C= MANE Select	ENSP00000361898.6:p.Ser166=
ENST00000372809.5:c.536C=	ENSP00000361895.5:p.Ser179=
ENST00000372811.9:c.497C=	ENSP00000361898.5:p.Ser166=
ENST00000420632.6:c.29C=	ENSP00000391261.2:p.Ser10=
ENST00000434861.5:c.491C=	ENSP00000407606.1:p.Ser164=
ENST00000469745.5:n.409C=
ENST00000480630.5:n.1144C=
ENST00000483824.5:n.632C=
NM_001136493.2:c.536C=	NP_001129965.1:p.Ser179=
NM_001287808.1:c.29C=	NP_001274737.1:p.Ser10=
NM_001287809.1:c.386C=	NP_001274738.1:p.Ser129=
NM_032793.4:c.497C=	NP_116182.2:p.Ser166=
NR_109896.1:n.678C=
XM_005271285.1:c.491C=	XP_005271342.1:p.Ser164=
XM_011542312.1:c.497C=	XP_011540614.1:p.Ser166=
XR_946783.1:n.645C=
NM_001349821.1:c.491C=	NP_001336750.1:p.Ser164=
NM_001349822.1:c.497C=	NP_001336751.1:p.Ser166=
NM_001349823.1:c.152C=	NP_001336752.1:p.Ser51=
NM_001136493.3:c.536C=	NP_001129965.1:p.Ser179=
NM_001287809.2:c.386C=	NP_001274738.1:p.Ser129=
NM_001349821.2:c.491C=	NP_001336750.1:p.Ser164=
NM_001349822.2:c.497C=	NP_001336751.1:p.Ser166=
NM_001349823.2:c.152C=	NP_001336752.1:p.Ser51=
NM_032793.5:c.497C= MANE Select	NP_116182.2:p.Ser166=
NR_109896.2:n.645C=
NM_001287808.2:c.29C=	NP_001274737.1:p.Ser10=