Canonical Allele Identifier: CA1144148455

Gene: MFSD2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39965491G= , CM000663.2:g.39965491G=	GRCh38
NC_000001.10:g.40431163G= , CM000663.1:g.40431163G=	GRCh37
NC_000001.9:g.40203750G=	NCBI36
NG_053084.1:g.15380G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372811.10:c.498G= MANE Select	ENSP00000361898.6:p.Ser166=
ENST00000372809.5:c.537G=	ENSP00000361895.5:p.Ser179=
ENST00000372811.9:c.498G=	ENSP00000361898.5:p.Ser166=
ENST00000420632.6:c.30G=	ENSP00000391261.2:p.Ser10=
ENST00000434861.5:c.492G=	ENSP00000407606.1:p.Ser164=
ENST00000469745.5:n.410G=
ENST00000480630.5:n.1145G=
ENST00000483824.5:n.633G=
NM_001136493.2:c.537G=	NP_001129965.1:p.Ser179=
NM_001287808.1:c.30G=	NP_001274737.1:p.Ser10=
NM_001287809.1:c.387G=	NP_001274738.1:p.Ser129=
NM_032793.4:c.498G=	NP_116182.2:p.Ser166=
NR_109896.1:n.679G=
XM_005271285.1:c.492G=	XP_005271342.1:p.Ser164=
XM_011542312.1:c.498G=	XP_011540614.1:p.Ser166=
XR_946783.1:n.646G=
NM_001349821.1:c.492G=	NP_001336750.1:p.Ser164=
NM_001349822.1:c.498G=	NP_001336751.1:p.Ser166=
NM_001349823.1:c.153G=	NP_001336752.1:p.Ser51=
NM_001136493.3:c.537G=	NP_001129965.1:p.Ser179=
NM_001287809.2:c.387G=	NP_001274738.1:p.Ser129=
NM_001349821.2:c.492G=	NP_001336750.1:p.Ser164=
NM_001349822.2:c.498G=	NP_001336751.1:p.Ser166=
NM_001349823.2:c.153G=	NP_001336752.1:p.Ser51=
NM_032793.5:c.498G= MANE Select	NP_116182.2:p.Ser166=
NR_109896.2:n.646G=
NM_001287808.2:c.30G=	NP_001274737.1:p.Ser10=