Canonical Allele Identifier: CA1164196320

Gene: MFSD2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39965477C= , CM000663.2:g.39965477C=	GRCh38
NC_000001.10:g.40431149C= , CM000663.1:g.40431149C=	GRCh37
NC_000001.9:g.40203736C=	NCBI36
NG_053084.1:g.15366C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372811.10:c.484C= MANE Select	ENSP00000361898.6:p.His162=
ENST00000372809.5:c.523C=	ENSP00000361895.5:p.His175=
ENST00000372811.9:c.484C=	ENSP00000361898.5:p.His162=
ENST00000420632.6:c.16C=	ENSP00000391261.2:p.His6=
ENST00000434861.5:c.478C=	ENSP00000407606.1:p.His160=
ENST00000469745.5:n.396C=
ENST00000480630.5:n.1131C=
ENST00000483824.5:n.619C=
NM_001136493.2:c.523C=	NP_001129965.1:p.His175=
NM_001287808.1:c.16C=	NP_001274737.1:p.His6=
NM_001287809.1:c.373C=	NP_001274738.1:p.His125=
NM_032793.4:c.484C=	NP_116182.2:p.His162=
NR_109896.1:n.665C=
XM_005271285.1:c.478C=	XP_005271342.1:p.His160=
XM_011542312.1:c.484C=	XP_011540614.1:p.His162=
XR_946783.1:n.632C=
NM_001349821.1:c.478C=	NP_001336750.1:p.His160=
NM_001349822.1:c.484C=	NP_001336751.1:p.His162=
NM_001349823.1:c.139C=	NP_001336752.1:p.His47=
NM_001136493.3:c.523C=	NP_001129965.1:p.His175=
NM_001287809.2:c.373C=	NP_001274738.1:p.His125=
NM_001349821.2:c.478C=	NP_001336750.1:p.His160=
NM_001349822.2:c.484C=	NP_001336751.1:p.His162=
NM_001349823.2:c.139C=	NP_001336752.1:p.His47=
NM_032793.5:c.484C= MANE Select	NP_116182.2:p.His162=
NR_109896.2:n.632C=
NM_001287808.2:c.16C=	NP_001274737.1:p.His6=