Canonical Allele Identifier: CA416360080

Gene: MTHFR

Linked Data

• MyVariant Identifiers: chr1:g.11861279G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11801222G>T , CM000663.2:g.11801222G>T	GRCh38
NC_000001.10:g.11861279G>T , CM000663.1:g.11861279G>T	GRCh37
NC_000001.9:g.11783866G>T	NCBI36
NG_008766.1:g.73G>T
NG_013351.1:g.9882C>A , LRG_726:g.9882C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376486.3:c.414C>A	ENSP00000365669.3:p.Ile138=
ENST00000376585.6:c.537C>A	ENSP00000365770.1:p.Ile179=
ENST00000376590.9:c.414C>A MANE Select	ENSP00000365775.3:p.Ile138=
ENST00000376592.6:c.414C>A	ENSP00000365777.1:p.Ile138=
ENST00000423400.7:c.534C>A	ENSP00000398908.3:p.Ile178=
ENST00000641407.1:c.414C>A	ENSP00000493098.1:p.Ile138=
ENST00000641437.1:n.546C>A
ENST00000641446.1:c.414C>A	ENSP00000493262.1:p.Ile138=
ENST00000641721.1:n.471C>A
ENST00000641747.1:c.237-900C>A	ENSP00000493116.1:n.237-900C>A
ENST00000641759.1:n.549C>A
ENST00000641805.1:n.697C>A
ENST00000641909.1:n.824C>A
ENST00000376583.7:c.537C>A	ENSP00000365767.3:p.Ile179=
ENST00000376585.5:c.537C>A	ENSP00000365770.1:p.Ile179=
ENST00000376590.7:c.414C>A	ENSP00000365775.3:p.Ile138=
ENST00000376592.5:c.414C>A	ENSP00000365777.1:p.Ile138=
ENST00000418034.1:c.414C>A	ENSP00000405082.1:p.Ile138=
NM_005957.4:c.414C>A , LRG_726t1:c.414C>A	NP_005948.3:p.Ile138=
XM_005263458.2:c.537C>A	XP_005263515.1:p.Ile179=
XM_005263460.3:c.414C>A	XP_005263517.1:p.Ile138=
XM_005263461.3:c.414C>A	XP_005263518.1:p.Ile138=
XM_005263462.3:c.414C>A	XP_005263519.1:p.Ile138=
XM_005263463.2:c.168C>A	XP_005263520.1:p.Ile56=
XM_011541495.1:c.534C>A	XP_011539797.1:p.Ile178=
XM_011541496.1:c.537C>A	XP_011539798.1:p.Ile179=
NM_001330358.1:c.537C>A	NP_001317287.1:p.Ile179=
XM_005263460.5:c.414C>A	XP_005263517.1:p.Ile138=
XM_005263462.4:c.414C>A	XP_005263519.1:p.Ile138=
XM_005263463.4:c.168C>A	XP_005263520.1:p.Ile56=
XM_011541495.3:c.534C>A	XP_011539797.1:p.Ile178=
XM_011541496.3:c.537C>A	XP_011539798.1:p.Ile179=
XM_017001328.2:c.537C>A	XP_016856817.1:p.Ile179=
XM_024447198.1:c.168C>A	XP_024302966.1:p.Ile56=
XR_002956640.1:n.1281C>A
NM_005957.5:c.414C>A MANE Select	NP_005948.3:p.Ile138=
NM_001330358.2:c.537C>A	NP_001317287.1:p.Ile179=