Canonical Allele Identifier: CA338421924

Gene: MTHFR

Linked Data

• MyVariant Identifiers: chr1:g.11860286A>T (hg19) ; chr1:g.11800229A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11800229A>T , CM000663.2:g.11800229A>T	GRCh38
NC_000001.10:g.11860286A>T , CM000663.1:g.11860286A>T	GRCh37
NC_000001.9:g.11782873A>T	NCBI36
NG_013351.1:g.10875T>A , LRG_726:g.10875T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376486.3:c.569T>A	ENSP00000365669.3:p.Phe190Tyr
ENST00000376585.6:c.692T>A	ENSP00000365770.1:p.Phe231Tyr
ENST00000376590.9:c.569T>A MANE Select	ENSP00000365775.3:p.Phe190Tyr
ENST00000376592.6:c.569T>A	ENSP00000365777.1:p.Phe190Tyr
ENST00000423400.7:c.689T>A	ENSP00000398908.3:p.Phe230Tyr
ENST00000641407.1:c.569T>A	ENSP00000493098.1:p.Phe190Tyr
ENST00000641437.1:n.1539T>A
ENST00000641446.1:c.569T>A	ENSP00000493262.1:p.Phe190Tyr
ENST00000641721.1:n.626T>A
ENST00000641747.1:c.*81T>A	ENSP00000493116.1:n.*81T>A
ENST00000641759.1:n.704T>A
ENST00000641805.1:n.852T>A
ENST00000641909.1:n.1817T>A
ENST00000376583.7:c.692T>A	ENSP00000365767.3:p.Phe231Tyr
ENST00000376585.5:c.692T>A	ENSP00000365770.1:p.Phe231Tyr
ENST00000376590.7:c.569T>A	ENSP00000365775.3:p.Phe190Tyr
ENST00000376592.5:c.569T>A	ENSP00000365777.1:p.Phe190Tyr
NM_005957.4:c.569T>A , LRG_726t1:c.569T>A	NP_005948.3:p.Phe190Tyr
XM_005263458.2:c.692T>A	XP_005263515.1:p.Phe231Tyr
XM_005263460.3:c.569T>A	XP_005263517.1:p.Phe190Tyr
XM_005263461.3:c.569T>A	XP_005263518.1:p.Phe190Tyr
XM_005263462.3:c.569T>A	XP_005263519.1:p.Phe190Tyr
XM_005263463.2:c.323T>A	XP_005263520.1:p.Phe108Tyr
XM_011541495.1:c.689T>A	XP_011539797.1:p.Phe230Tyr
XM_011541496.1:c.692T>A	XP_011539798.1:p.Phe231Tyr
NM_001330358.1:c.692T>A	NP_001317287.1:p.Phe231Tyr
XM_005263460.5:c.569T>A	XP_005263517.1:p.Phe190Tyr
XM_005263462.4:c.569T>A	XP_005263519.1:p.Phe190Tyr
XM_005263463.4:c.323T>A	XP_005263520.1:p.Phe108Tyr
XM_011541495.3:c.689T>A	XP_011539797.1:p.Phe230Tyr
XM_011541496.3:c.692T>A	XP_011539798.1:p.Phe231Tyr
XM_017001328.2:c.692T>A	XP_016856817.1:p.Phe231Tyr
XM_024447198.1:c.323T>A	XP_024302966.1:p.Phe108Tyr
XR_002956640.1:n.1436T>A
NM_005957.5:c.569T>A MANE Select	NP_005948.3:p.Phe190Tyr
NM_001330358.2:c.692T>A	NP_001317287.1:p.Phe231Tyr