Canonical Allele Identifier: CA1153801635

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11795373_11795374delinsGC , CM000663.2:g.11795373_11795374delinsGC	GRCh38
NC_000001.10:g.11855430_11855431delinsGC , CM000663.1:g.11855430_11855431delinsGC	GRCh37
NC_000001.9:g.11778017_11778018delinsGC	NCBI36
NG_013351.1:g.15730_15731delinsGC , LRG_726:g.15730_15731delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.904-26_904-25delinsGC	ENSP00000365770.1:n.904-26_904-25delinsGC
ENST00000376590.9:c.781-26_781-25delinsGC MANE Select	ENSP00000365775.3:n.781-26_781-25delinsGC
ENST00000376592.6:c.781-26_781-25delinsGC	ENSP00000365777.1:n.781-26_781-25delinsGC
ENST00000423400.7:c.901-26_901-25delinsGC	ENSP00000398908.3:n.901-26_901-25delinsGC
ENST00000641407.1:c.781-26_781-25delinsGC	ENSP00000493098.1:n.781-26_781-25delinsGC
ENST00000641446.1:c.781-26_781-25delinsGC	ENSP00000493262.1:n.781-26_781-25delinsGC
ENST00000641721.1:n.644-26_644-25delinsGC
ENST00000641747.1:c.*293-26_*293-25delinsGC	ENSP00000493116.1:n.*293-26_*293-25delinsGC
ENST00000641759.1:n.916-26_916-25delinsGC
ENST00000641805.1:n.1064-26_1064-25delinsGC
ENST00000641820.1:c.46-26_46-25delinsGC	ENSP00000492937.1:n.46-26_46-25delinsGC
ENST00000376583.7:c.904-26_904-25delinsGC	ENSP00000365767.3:n.904-26_904-25delinsGC
ENST00000376585.5:c.904-26_904-25delinsGC	ENSP00000365770.1:n.904-26_904-25delinsGC
ENST00000376590.7:c.781-26_781-25delinsGC	ENSP00000365775.3:n.781-26_781-25delinsGC
ENST00000376592.5:c.781-26_781-25delinsGC	ENSP00000365777.1:n.781-26_781-25delinsGC
NM_005957.4:c.781-26_781-25delinsGC , LRG_726t1:c.781-26_781-25delinsGC	NP_005948.3:n.781-26_781-25delinsGC
XM_005263458.2:c.904-26_904-25delinsGC	XP_005263515.1:n.904-26_904-25delinsGC
XM_005263460.3:c.781-26_781-25delinsGC	XP_005263517.1:n.781-26_781-25delinsGC
XM_005263461.3:c.781-26_781-25delinsGC	XP_005263518.1:n.781-26_781-25delinsGC
XM_005263462.3:c.781-26_781-25delinsGC	XP_005263519.1:n.781-26_781-25delinsGC
XM_005263463.2:c.535-26_535-25delinsGC	XP_005263520.1:n.535-26_535-25delinsGC
XM_011541495.1:c.901-26_901-25delinsGC	XP_011539797.1:n.901-26_901-25delinsGC
XM_011541496.1:c.904-26_904-25delinsGC	XP_011539798.1:n.904-26_904-25delinsGC
NM_001330358.1:c.904-26_904-25delinsGC	NP_001317287.1:n.904-26_904-25delinsGC
XM_005263460.5:c.781-26_781-25delinsGC	XP_005263517.1:n.781-26_781-25delinsGC
XM_005263462.4:c.781-26_781-25delinsGC	XP_005263519.1:n.781-26_781-25delinsGC
XM_005263463.4:c.535-26_535-25delinsGC	XP_005263520.1:n.535-26_535-25delinsGC
XM_011541495.3:c.901-26_901-25delinsGC	XP_011539797.1:n.901-26_901-25delinsGC
XM_011541496.3:c.904-26_904-25delinsGC	XP_011539798.1:n.904-26_904-25delinsGC
XM_017001328.2:c.904-26_904-25delinsGC	XP_016856817.1:n.904-26_904-25delinsGC
XM_024447198.1:c.535-26_535-25delinsGC	XP_024302966.1:n.535-26_535-25delinsGC
XR_002956640.1:n.1648-26_1648-25delinsGC
NM_005957.5:c.781-26_781-25delinsGC MANE Select	NP_005948.3:n.781-26_781-25delinsGC
NM_001330358.2:c.904-26_904-25delinsGC	NP_001317287.1:n.904-26_904-25delinsGC