Canonical Allele Identifier: CA2559133627

Gene: MFSD2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39965575C>G , CM000663.2:g.39965575C>G	GRCh38
NC_000001.10:g.40431247C>G , CM000663.1:g.40431247C>G	GRCh37
NC_000001.9:g.40203834C>G	NCBI36
NG_053084.1:g.15464C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372811.10:c.556+26C>G MANE Select	ENSP00000361898.6:n.556+26C>G
ENST00000372809.5:c.595+26C>G	ENSP00000361895.5:n.595+26C>G
ENST00000372811.9:c.556+26C>G	ENSP00000361898.5:n.556+26C>G
ENST00000420632.6:c.88+26C>G	ENSP00000391261.2:n.88+26C>G
ENST00000434861.5:c.550+26C>G	ENSP00000407606.1:n.550+26C>G
ENST00000469745.5:n.468+26C>G
ENST00000480630.5:n.1203+26C>G
ENST00000483824.5:n.691+26C>G
NM_001136493.2:c.595+26C>G	NP_001129965.1:n.595+26C>G
NM_001287808.1:c.88+26C>G	NP_001274737.1:n.88+26C>G
NM_001287809.1:c.445+26C>G	NP_001274738.1:n.445+26C>G
NM_032793.4:c.556+26C>G	NP_116182.2:n.556+26C>G
NR_109896.1:n.737+26C>G
XM_005271285.1:c.550+26C>G	XP_005271342.1:n.550+26C>G
XM_011542312.1:c.556+26C>G	XP_011540614.1:n.556+26C>G
XR_946783.1:n.704+26C>G
NM_001349821.1:c.550+26C>G	NP_001336750.1:n.550+26C>G
NM_001349822.1:c.556+26C>G	NP_001336751.1:n.556+26C>G
NM_001349823.1:c.211+26C>G	NP_001336752.1:n.211+26C>G
NM_001136493.3:c.595+26C>G	NP_001129965.1:n.595+26C>G
NM_001287809.2:c.445+26C>G	NP_001274738.1:n.445+26C>G
NM_001349821.2:c.550+26C>G	NP_001336750.1:n.550+26C>G
NM_001349822.2:c.556+26C>G	NP_001336751.1:n.556+26C>G
NM_001349823.2:c.211+26C>G	NP_001336752.1:n.211+26C>G
NM_032793.5:c.556+26C>G MANE Select	NP_116182.2:n.556+26C>G
NR_109896.2:n.704+26C>G
NM_001287808.2:c.88+26C>G	NP_001274737.1:n.88+26C>G