Canonical Allele Identifier: CA339834954

Gene: MFSD2A

Linked Data

• MyVariant Identifiers: chr1:g.40431195C>A (hg19) ; chr1:g.39965523C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39965523C>A , CM000663.2:g.39965523C>A	GRCh38
NC_000001.10:g.40431195C>A , CM000663.1:g.40431195C>A	GRCh37
NC_000001.9:g.40203782C>A	NCBI36
NG_053084.1:g.15412C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372811.10:c.530C>A MANE Select	ENSP00000361898.6:p.Thr177Asn
ENST00000372809.5:c.569C>A	ENSP00000361895.5:p.Thr190Asn
ENST00000372811.9:c.530C>A	ENSP00000361898.5:p.Thr177Asn
ENST00000420632.6:c.62C>A	ENSP00000391261.2:p.Thr21Asn
ENST00000434861.5:c.524C>A	ENSP00000407606.1:p.Thr175Asn
ENST00000469745.5:n.442C>A
ENST00000480630.5:n.1177C>A
ENST00000483824.5:n.665C>A
NM_001136493.2:c.569C>A	NP_001129965.1:p.Thr190Asn
NM_001287808.1:c.62C>A	NP_001274737.1:p.Thr21Asn
NM_001287809.1:c.419C>A	NP_001274738.1:p.Thr140Asn
NM_032793.4:c.530C>A	NP_116182.2:p.Thr177Asn
NR_109896.1:n.711C>A
XM_005271285.1:c.524C>A	XP_005271342.1:p.Thr175Asn
XM_011542312.1:c.530C>A	XP_011540614.1:p.Thr177Asn
XR_946783.1:n.678C>A
NM_001349821.1:c.524C>A	NP_001336750.1:p.Thr175Asn
NM_001349822.1:c.530C>A	NP_001336751.1:p.Thr177Asn
NM_001349823.1:c.185C>A	NP_001336752.1:p.Thr62Asn
NM_001136493.3:c.569C>A	NP_001129965.1:p.Thr190Asn
NM_001287809.2:c.419C>A	NP_001274738.1:p.Thr140Asn
NM_001349821.2:c.524C>A	NP_001336750.1:p.Thr175Asn
NM_001349822.2:c.530C>A	NP_001336751.1:p.Thr177Asn
NM_001349823.2:c.185C>A	NP_001336752.1:p.Thr62Asn
NM_032793.5:c.530C>A MANE Select	NP_116182.2:p.Thr177Asn
NR_109896.2:n.678C>A
NM_001287808.2:c.62C>A	NP_001274737.1:p.Thr21Asn