Canonical Allele Identifier: CA1153798744

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11794399_11794401delinsCGA , CM000663.2:g.11794399_11794401delinsCGA	GRCh38
NC_000001.10:g.11854456_11854458delinsCGA , CM000663.1:g.11854456_11854458delinsCGA	GRCh37
NC_000001.9:g.11777043_11777045delinsCGA	NCBI36
NG_013351.1:g.16703_16705delinsTCG , LRG_726:g.16703_16705delinsTCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000376585.6:c.1427_1429delinsTCG	ENSP00000365770.1:p.Phe476=
ENST00000376590.9:c.1304_1306delinsTCG MANE Select	ENSP00000365775.3:p.Phe435=
ENST00000376592.6:c.1304_1306delinsTCG	ENSP00000365777.1:p.Phe435=
ENST00000423400.7:c.1424_1426delinsTCG	ENSP00000398908.3:p.Phe475=
ENST00000641407.1:c.1304_1306delinsTCG	ENSP00000493098.1:p.Phe435=
ENST00000641446.1:c.1304_1306delinsTCG	ENSP00000493262.1:p.Phe435=
ENST00000641747.1:c.*816_*818delinsTCG	ENSP00000493116.1:n.*816_*818delinsTCG
ENST00000641759.1:n.1673_1675delinsTCG
ENST00000641805.1:n.1821_1823delinsTCG
ENST00000641820.1:c.569_571delinsTCG	ENSP00000492937.1:p.Phe190=
ENST00000376583.7:c.1427_1429delinsTCG	ENSP00000365767.3:p.Phe476=
ENST00000376585.5:c.1427_1429delinsTCG	ENSP00000365770.1:p.Phe476=
ENST00000376590.7:c.1304_1306delinsTCG	ENSP00000365775.3:p.Phe435=
ENST00000376592.5:c.1304_1306delinsTCG	ENSP00000365777.1:p.Phe435=
NM_005957.4:c.1304_1306delinsTCG , LRG_726t1:c.1304_1306delinsTCG	NP_005948.3:p.Phe435=
XM_005263458.2:c.1427_1429delinsTCG	XP_005263515.1:p.Phe476=
XM_005263460.3:c.1304_1306delinsTCG	XP_005263517.1:p.Phe435=
XM_005263461.3:c.1304_1306delinsTCG	XP_005263518.1:p.Phe435=
XM_005263462.3:c.1304_1306delinsTCG	XP_005263519.1:p.Phe435=
XM_005263463.2:c.1058_1060delinsTCG	XP_005263520.1:p.Phe353=
XM_011541495.1:c.1424_1426delinsTCG	XP_011539797.1:p.Phe475=
XM_011541496.1:c.1427_1429delinsTCG	XP_011539798.1:p.Phe476=
NM_001330358.1:c.1427_1429delinsTCG	NP_001317287.1:p.Phe476=
XM_005263460.5:c.1304_1306delinsTCG	XP_005263517.1:p.Phe435=
XM_005263462.4:c.1304_1306delinsTCG	XP_005263519.1:p.Phe435=
XM_005263463.4:c.1058_1060delinsTCG	XP_005263520.1:p.Phe353=
XM_011541495.3:c.1424_1426delinsTCG	XP_011539797.1:p.Phe475=
XM_011541496.3:c.1427_1429delinsTCG	XP_011539798.1:p.Phe476=
XM_017001328.2:c.1427_1429delinsTCG	XP_016856817.1:p.Phe476=
XM_024447198.1:c.1058_1060delinsTCG	XP_024302966.1:p.Phe353=
XR_002956640.1:n.2405_2407delinsTCG
NM_005957.5:c.1304_1306delinsTCG MANE Select	NP_005948.3:p.Phe435=
NM_001330358.2:c.1427_1429delinsTCG	NP_001317287.1:p.Phe476=