Canonical Allele Identifier: CA1164196373

Gene: MFSD2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39965525G= , CM000663.2:g.39965525G=	GRCh38
NC_000001.10:g.40431197G= , CM000663.1:g.40431197G=	GRCh37
NC_000001.9:g.40203784G=	NCBI36
NG_053084.1:g.15414G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372811.10:c.532G= MANE Select	ENSP00000361898.6:p.Glu178=
ENST00000372809.5:c.571G=	ENSP00000361895.5:p.Glu191=
ENST00000372811.9:c.532G=	ENSP00000361898.5:p.Glu178=
ENST00000420632.6:c.64G=	ENSP00000391261.2:p.Glu22=
ENST00000434861.5:c.526G=	ENSP00000407606.1:p.Glu176=
ENST00000469745.5:n.444G=
ENST00000480630.5:n.1179G=
ENST00000483824.5:n.667G=
NM_001136493.2:c.571G=	NP_001129965.1:p.Glu191=
NM_001287808.1:c.64G=	NP_001274737.1:p.Glu22=
NM_001287809.1:c.421G=	NP_001274738.1:p.Glu141=
NM_032793.4:c.532G=	NP_116182.2:p.Glu178=
NR_109896.1:n.713G=
XM_005271285.1:c.526G=	XP_005271342.1:p.Glu176=
XM_011542312.1:c.532G=	XP_011540614.1:p.Glu178=
XR_946783.1:n.680G=
NM_001349821.1:c.526G=	NP_001336750.1:p.Glu176=
NM_001349822.1:c.532G=	NP_001336751.1:p.Glu178=
NM_001349823.1:c.187G=	NP_001336752.1:p.Glu63=
NM_001136493.3:c.571G=	NP_001129965.1:p.Glu191=
NM_001287809.2:c.421G=	NP_001274738.1:p.Glu141=
NM_001349821.2:c.526G=	NP_001336750.1:p.Glu176=
NM_001349822.2:c.532G=	NP_001336751.1:p.Glu178=
NM_001349823.2:c.187G=	NP_001336752.1:p.Glu63=
NM_032793.5:c.532G= MANE Select	NP_116182.2:p.Glu178=
NR_109896.2:n.680G=
NM_001287808.2:c.64G=	NP_001274737.1:p.Glu22=