Canonical Allele Identifier: CA1164196410

Gene: MFSD2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39965547A= , CM000663.2:g.39965547A=	GRCh38
NC_000001.10:g.40431219A= , CM000663.1:g.40431219A=	GRCh37
NC_000001.9:g.40203806A=	NCBI36
NG_053084.1:g.15436A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372811.10:c.554A= MANE Select	ENSP00000361898.6:p.Tyr185=
ENST00000372809.5:c.593A=	ENSP00000361895.5:p.Tyr198=
ENST00000372811.9:c.554A=	ENSP00000361898.5:p.Tyr185=
ENST00000420632.6:c.86A=	ENSP00000391261.2:p.Tyr29=
ENST00000434861.5:c.548A=	ENSP00000407606.1:p.Tyr183=
ENST00000469745.5:n.466A=
ENST00000480630.5:n.1201A=
ENST00000483824.5:n.689A=
NM_001136493.2:c.593A=	NP_001129965.1:p.Tyr198=
NM_001287808.1:c.86A=	NP_001274737.1:p.Tyr29=
NM_001287809.1:c.443A=	NP_001274738.1:p.Tyr148=
NM_032793.4:c.554A=	NP_116182.2:p.Tyr185=
NR_109896.1:n.735A=
XM_005271285.1:c.548A=	XP_005271342.1:p.Tyr183=
XM_011542312.1:c.554A=	XP_011540614.1:p.Tyr185=
XR_946783.1:n.702A=
NM_001349821.1:c.548A=	NP_001336750.1:p.Tyr183=
NM_001349822.1:c.554A=	NP_001336751.1:p.Tyr185=
NM_001349823.1:c.209A=	NP_001336752.1:p.Tyr70=
NM_001136493.3:c.593A=	NP_001129965.1:p.Tyr198=
NM_001287809.2:c.443A=	NP_001274738.1:p.Tyr148=
NM_001349821.2:c.548A=	NP_001336750.1:p.Tyr183=
NM_001349822.2:c.554A=	NP_001336751.1:p.Tyr185=
NM_001349823.2:c.209A=	NP_001336752.1:p.Tyr70=
NM_032793.5:c.554A= MANE Select	NP_116182.2:p.Tyr185=
NR_109896.2:n.702A=
NM_001287808.2:c.86A=	NP_001274737.1:p.Tyr29=