Canonical Allele Identifier: CA1164196364

Gene: MFSD2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39965522A= , CM000663.2:g.39965522A=	GRCh38
NC_000001.10:g.40431194A= , CM000663.1:g.40431194A=	GRCh37
NC_000001.9:g.40203781A=	NCBI36
NG_053084.1:g.15411A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372811.10:c.529A= MANE Select	ENSP00000361898.6:p.Thr177=
ENST00000372809.5:c.568A=	ENSP00000361895.5:p.Thr190=
ENST00000372811.9:c.529A=	ENSP00000361898.5:p.Thr177=
ENST00000420632.6:c.61A=	ENSP00000391261.2:p.Thr21=
ENST00000434861.5:c.523A=	ENSP00000407606.1:p.Thr175=
ENST00000469745.5:n.441A=
ENST00000480630.5:n.1176A=
ENST00000483824.5:n.664A=
NM_001136493.2:c.568A=	NP_001129965.1:p.Thr190=
NM_001287808.1:c.61A=	NP_001274737.1:p.Thr21=
NM_001287809.1:c.418A=	NP_001274738.1:p.Thr140=
NM_032793.4:c.529A=	NP_116182.2:p.Thr177=
NR_109896.1:n.710A=
XM_005271285.1:c.523A=	XP_005271342.1:p.Thr175=
XM_011542312.1:c.529A=	XP_011540614.1:p.Thr177=
XR_946783.1:n.677A=
NM_001349821.1:c.523A=	NP_001336750.1:p.Thr175=
NM_001349822.1:c.529A=	NP_001336751.1:p.Thr177=
NM_001349823.1:c.184A=	NP_001336752.1:p.Thr62=
NM_001136493.3:c.568A=	NP_001129965.1:p.Thr190=
NM_001287809.2:c.418A=	NP_001274738.1:p.Thr140=
NM_001349821.2:c.523A=	NP_001336750.1:p.Thr175=
NM_001349822.2:c.529A=	NP_001336751.1:p.Thr177=
NM_001349823.2:c.184A=	NP_001336752.1:p.Thr62=
NM_032793.5:c.529A= MANE Select	NP_116182.2:p.Thr177=
NR_109896.2:n.677A=
NM_001287808.2:c.61A=	NP_001274737.1:p.Thr21=