Canonical Allele Identifier: CA2743288252

Gene: MFSD2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39965395C>A , CM000663.2:g.39965395C>A	GRCh38
NC_000001.10:g.40431067C>A , CM000663.1:g.40431067C>A	GRCh37
NC_000001.9:g.40203654C>A	NCBI36
NG_053084.1:g.15284C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372811.10:c.477+61C>A MANE Select	ENSP00000361898.6:n.477+61C>A
ENST00000372809.5:c.516+61C>A	ENSP00000361895.5:n.516+61C>A
ENST00000372811.9:c.477+61C>A	ENSP00000361898.5:n.477+61C>A
ENST00000420632.6:c.9+61C>A	ENSP00000391261.2:n.9+61C>A
ENST00000434861.5:c.471+61C>A	ENSP00000407606.1:n.471+61C>A
ENST00000469745.5:n.389+61C>A
ENST00000480630.5:n.1124+61C>A
ENST00000483824.5:n.612+61C>A
NM_001136493.2:c.516+61C>A	NP_001129965.1:n.516+61C>A
NM_001287808.1:c.9+61C>A	NP_001274737.1:n.9+61C>A
NM_001287809.1:c.366+61C>A	NP_001274738.1:n.366+61C>A
NM_032793.4:c.477+61C>A	NP_116182.2:n.477+61C>A
NR_109896.1:n.658+61C>A
XM_005271285.1:c.471+61C>A	XP_005271342.1:n.471+61C>A
XM_011542312.1:c.477+61C>A	XP_011540614.1:n.477+61C>A
XR_946783.1:n.625+61C>A
NM_001349821.1:c.471+61C>A	NP_001336750.1:n.471+61C>A
NM_001349822.1:c.477+61C>A	NP_001336751.1:n.477+61C>A
NM_001349823.1:c.132+61C>A	NP_001336752.1:n.132+61C>A
NM_001136493.3:c.516+61C>A	NP_001129965.1:n.516+61C>A
NM_001287809.2:c.366+61C>A	NP_001274738.1:n.366+61C>A
NM_001349821.2:c.471+61C>A	NP_001336750.1:n.471+61C>A
NM_001349822.2:c.477+61C>A	NP_001336751.1:n.477+61C>A
NM_001349823.2:c.132+61C>A	NP_001336752.1:n.132+61C>A
NM_032793.5:c.477+61C>A MANE Select	NP_116182.2:n.477+61C>A
NR_109896.2:n.625+61C>A
NM_001287808.2:c.9+61C>A	NP_001274737.1:n.9+61C>A