Canonical Allele Identifier: CA338422015

Gene: MTHFR

Linked Data

• MyVariant Identifiers: chr1:g.11860326C>T (hg19) ; chr1:g.11800269C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11800269C>T , CM000663.2:g.11800269C>T	GRCh38
NC_000001.10:g.11860326C>T , CM000663.1:g.11860326C>T	GRCh37
NC_000001.9:g.11782913C>T	NCBI36
NG_013351.1:g.10835G>A , LRG_726:g.10835G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376486.3:c.529G>A	ENSP00000365669.3:p.Asp177Asn
ENST00000376585.6:c.652G>A	ENSP00000365770.1:p.Asp218Asn
ENST00000376590.9:c.529G>A MANE Select	ENSP00000365775.3:p.Asp177Asn
ENST00000376592.6:c.529G>A	ENSP00000365777.1:p.Asp177Asn
ENST00000423400.7:c.649G>A	ENSP00000398908.3:p.Asp217Asn
ENST00000641407.1:c.529G>A	ENSP00000493098.1:p.Asp177Asn
ENST00000641437.1:n.1499G>A
ENST00000641446.1:c.529G>A	ENSP00000493262.1:p.Asp177Asn
ENST00000641721.1:n.586G>A
ENST00000641747.1:c.*41G>A	ENSP00000493116.1:n.*41G>A
ENST00000641759.1:n.664G>A
ENST00000641805.1:n.812G>A
ENST00000641909.1:n.1777G>A
ENST00000376583.7:c.652G>A	ENSP00000365767.3:p.Asp218Asn
ENST00000376585.5:c.652G>A	ENSP00000365770.1:p.Asp218Asn
ENST00000376590.7:c.529G>A	ENSP00000365775.3:p.Asp177Asn
ENST00000376592.5:c.529G>A	ENSP00000365777.1:p.Asp177Asn
NM_005957.4:c.529G>A , LRG_726t1:c.529G>A	NP_005948.3:p.Asp177Asn
XM_005263458.2:c.652G>A	XP_005263515.1:p.Asp218Asn
XM_005263460.3:c.529G>A	XP_005263517.1:p.Asp177Asn
XM_005263461.3:c.529G>A	XP_005263518.1:p.Asp177Asn
XM_005263462.3:c.529G>A	XP_005263519.1:p.Asp177Asn
XM_005263463.2:c.283G>A	XP_005263520.1:p.Asp95Asn
XM_011541495.1:c.649G>A	XP_011539797.1:p.Asp217Asn
XM_011541496.1:c.652G>A	XP_011539798.1:p.Asp218Asn
NM_001330358.1:c.652G>A	NP_001317287.1:p.Asp218Asn
XM_005263460.5:c.529G>A	XP_005263517.1:p.Asp177Asn
XM_005263462.4:c.529G>A	XP_005263519.1:p.Asp177Asn
XM_005263463.4:c.283G>A	XP_005263520.1:p.Asp95Asn
XM_011541495.3:c.649G>A	XP_011539797.1:p.Asp217Asn
XM_011541496.3:c.652G>A	XP_011539798.1:p.Asp218Asn
XM_017001328.2:c.652G>A	XP_016856817.1:p.Asp218Asn
XM_024447198.1:c.283G>A	XP_024302966.1:p.Asp95Asn
XR_002956640.1:n.1396G>A
NM_005957.5:c.529G>A MANE Select	NP_005948.3:p.Asp177Asn
NM_001330358.2:c.652G>A	NP_001317287.1:p.Asp218Asn