Canonical Allele Identifier: CA1153799908

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11794779_11794780delinsCT , CM000663.2:g.11794779_11794780delinsCT	GRCh38
NC_000001.10:g.11854836_11854837delinsCT , CM000663.1:g.11854836_11854837delinsCT	GRCh37
NC_000001.9:g.11777423_11777424delinsCT	NCBI36
NG_013351.1:g.16324_16325delinsAG , LRG_726:g.16324_16325delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000376585.6:c.1238_1239delinsAG	ENSP00000365770.1:p.Lys413=
ENST00000376590.9:c.1115_1116delinsAG MANE Select	ENSP00000365775.3:p.Lys372=
ENST00000376592.6:c.1115_1116delinsAG	ENSP00000365777.1:p.Lys372=
ENST00000423400.7:c.1235_1236delinsAG	ENSP00000398908.3:p.Lys412=
ENST00000641407.1:c.1115_1116delinsAG	ENSP00000493098.1:p.Lys372=
ENST00000641446.1:c.1115_1116delinsAG	ENSP00000493262.1:p.Lys372=
ENST00000641747.1:c.*627_*628delinsAG	ENSP00000493116.1:n.*627_*628delinsAG
ENST00000641759.1:n.1484_1485delinsAG
ENST00000641805.1:n.1632_1633delinsAG
ENST00000641820.1:c.380_381delinsAG	ENSP00000492937.1:p.Lys127=
ENST00000376583.7:c.1238_1239delinsAG	ENSP00000365767.3:p.Lys413=
ENST00000376585.5:c.1238_1239delinsAG	ENSP00000365770.1:p.Lys413=
ENST00000376590.7:c.1115_1116delinsAG	ENSP00000365775.3:p.Lys372=
ENST00000376592.5:c.1115_1116delinsAG	ENSP00000365777.1:p.Lys372=
NM_005957.4:c.1115_1116delinsAG , LRG_726t1:c.1115_1116delinsAG	NP_005948.3:p.Lys372=
XM_005263458.2:c.1238_1239delinsAG	XP_005263515.1:p.Lys413=
XM_005263460.3:c.1115_1116delinsAG	XP_005263517.1:p.Lys372=
XM_005263461.3:c.1115_1116delinsAG	XP_005263518.1:p.Lys372=
XM_005263462.3:c.1115_1116delinsAG	XP_005263519.1:p.Lys372=
XM_005263463.2:c.869_870delinsAG	XP_005263520.1:p.Lys290=
XM_011541495.1:c.1235_1236delinsAG	XP_011539797.1:p.Lys412=
XM_011541496.1:c.1238_1239delinsAG	XP_011539798.1:p.Lys413=
NM_001330358.1:c.1238_1239delinsAG	NP_001317287.1:p.Lys413=
XM_005263460.5:c.1115_1116delinsAG	XP_005263517.1:p.Lys372=
XM_005263462.4:c.1115_1116delinsAG	XP_005263519.1:p.Lys372=
XM_005263463.4:c.869_870delinsAG	XP_005263520.1:p.Lys290=
XM_011541495.3:c.1235_1236delinsAG	XP_011539797.1:p.Lys412=
XM_011541496.3:c.1238_1239delinsAG	XP_011539798.1:p.Lys413=
XM_017001328.2:c.1238_1239delinsAG	XP_016856817.1:p.Lys413=
XM_024447198.1:c.869_870delinsAG	XP_024302966.1:p.Lys290=
XR_002956640.1:n.2216_2217delinsAG
NM_005957.5:c.1115_1116delinsAG MANE Select	NP_005948.3:p.Lys372=
NM_001330358.2:c.1238_1239delinsAG	NP_001317287.1:p.Lys413=