Canonical Allele Identifier: CA1164196408

Gene: MFSD2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39965545C= , CM000663.2:g.39965545C=	GRCh38
NC_000001.10:g.40431217C= , CM000663.1:g.40431217C=	GRCh37
NC_000001.9:g.40203804C=	NCBI36
NG_053084.1:g.15434C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372811.10:c.552C= MANE Select	ENSP00000361898.6:p.Ala184=
ENST00000372809.5:c.591C=	ENSP00000361895.5:p.Ala197=
ENST00000372811.9:c.552C=	ENSP00000361898.5:p.Ala184=
ENST00000420632.6:c.84C=	ENSP00000391261.2:p.Ala28=
ENST00000434861.5:c.546C=	ENSP00000407606.1:p.Ala182=
ENST00000469745.5:n.464C=
ENST00000480630.5:n.1199C=
ENST00000483824.5:n.687C=
NM_001136493.2:c.591C=	NP_001129965.1:p.Ala197=
NM_001287808.1:c.84C=	NP_001274737.1:p.Ala28=
NM_001287809.1:c.441C=	NP_001274738.1:p.Ala147=
NM_032793.4:c.552C=	NP_116182.2:p.Ala184=
NR_109896.1:n.733C=
XM_005271285.1:c.546C=	XP_005271342.1:p.Ala182=
XM_011542312.1:c.552C=	XP_011540614.1:p.Ala184=
XR_946783.1:n.700C=
NM_001349821.1:c.546C=	NP_001336750.1:p.Ala182=
NM_001349822.1:c.552C=	NP_001336751.1:p.Ala184=
NM_001349823.1:c.207C=	NP_001336752.1:p.Ala69=
NM_001136493.3:c.591C=	NP_001129965.1:p.Ala197=
NM_001287809.2:c.441C=	NP_001274738.1:p.Ala147=
NM_001349821.2:c.546C=	NP_001336750.1:p.Ala182=
NM_001349822.2:c.552C=	NP_001336751.1:p.Ala184=
NM_001349823.2:c.207C=	NP_001336752.1:p.Ala69=
NM_032793.5:c.552C= MANE Select	NP_116182.2:p.Ala184=
NR_109896.2:n.700C=
NM_001287808.2:c.84C=	NP_001274737.1:p.Ala28=