Canonical Allele Identifier: CA339835021

Gene: MFSD2A

Linked Data

• MyVariant Identifiers: chr1:g.40431203G>T (hg19) ; chr1:g.39965531G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39965531G>T , CM000663.2:g.39965531G>T	GRCh38
NC_000001.10:g.40431203G>T , CM000663.1:g.40431203G>T	GRCh37
NC_000001.9:g.40203790G>T	NCBI36
NG_053084.1:g.15420G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372811.10:c.538G>T MANE Select	ENSP00000361898.6:p.Asp180Tyr
ENST00000372809.5:c.577G>T	ENSP00000361895.5:p.Asp193Tyr
ENST00000372811.9:c.538G>T	ENSP00000361898.5:p.Asp180Tyr
ENST00000420632.6:c.70G>T	ENSP00000391261.2:p.Asp24Tyr
ENST00000434861.5:c.532G>T	ENSP00000407606.1:p.Asp178Tyr
ENST00000469745.5:n.450G>T
ENST00000480630.5:n.1185G>T
ENST00000483824.5:n.673G>T
NM_001136493.2:c.577G>T	NP_001129965.1:p.Asp193Tyr
NM_001287808.1:c.70G>T	NP_001274737.1:p.Asp24Tyr
NM_001287809.1:c.427G>T	NP_001274738.1:p.Asp143Tyr
NM_032793.4:c.538G>T	NP_116182.2:p.Asp180Tyr
NR_109896.1:n.719G>T
XM_005271285.1:c.532G>T	XP_005271342.1:p.Asp178Tyr
XM_011542312.1:c.538G>T	XP_011540614.1:p.Asp180Tyr
XR_946783.1:n.686G>T
NM_001349821.1:c.532G>T	NP_001336750.1:p.Asp178Tyr
NM_001349822.1:c.538G>T	NP_001336751.1:p.Asp180Tyr
NM_001349823.1:c.193G>T	NP_001336752.1:p.Asp65Tyr
NM_001136493.3:c.577G>T	NP_001129965.1:p.Asp193Tyr
NM_001287809.2:c.427G>T	NP_001274738.1:p.Asp143Tyr
NM_001349821.2:c.532G>T	NP_001336750.1:p.Asp178Tyr
NM_001349822.2:c.538G>T	NP_001336751.1:p.Asp180Tyr
NM_001349823.2:c.193G>T	NP_001336752.1:p.Asp65Tyr
NM_032793.5:c.538G>T MANE Select	NP_116182.2:p.Asp180Tyr
NR_109896.2:n.686G>T
NM_001287808.2:c.70G>T	NP_001274737.1:p.Asp24Tyr