Canonical Allele Identifier: CA1153792307

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11791151_11791155delinsATCCC , CM000663.2:g.11791151_11791155delinsATCCC	GRCh38
NC_000001.10:g.11851208_11851212delinsATCCC , CM000663.1:g.11851208_11851212delinsATCCC	GRCh37
NC_000001.9:g.11773795_11773799delinsATCCC	NCBI36
NG_013351.1:g.19949_19953delinsGGGAT , LRG_726:g.19949_19953delinsGGGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.1875+52_1875+56delinsGGGAT	ENSP00000365770.1:n.1875+52_1875+56delinsGGGAT
ENST00000376590.9:c.1752+52_1752+56delinsGGGAT MANE Select	ENSP00000365775.3:n.1752+52_1752+56delinsGGGAT
ENST00000376592.6:c.1752+52_1752+56delinsGGGAT	ENSP00000365777.1:n.1752+52_1752+56delinsGGGAT
ENST00000423400.7:c.1872+52_1872+56delinsGGGAT	ENSP00000398908.3:n.1872+52_1872+56delinsGGGAT
ENST00000641407.1:c.1752+52_1752+56delinsGGGAT	ENSP00000493098.1:n.1752+52_1752+56delinsGGGAT
ENST00000641446.1:c.*211+52_*211+56delinsGGGAT	ENSP00000493262.1:n.*211+52_*211+56delinsGGGAT
ENST00000641747.1:c.*1264+52_*1264+56delinsGGGAT	ENSP00000493116.1:n.*1264+52_*1264+56delinsGGGAT
ENST00000641759.1:n.2121+52_2121+56delinsGGGAT
ENST00000641805.1:n.2269+52_2269+56delinsGGGAT
ENST00000641820.1:c.1017+52_1017+56delinsGGGAT	ENSP00000492937.1:n.1017+52_1017+56delinsGGGAT
ENST00000376583.7:c.1875+52_1875+56delinsGGGAT	ENSP00000365767.3:n.1875+52_1875+56delinsGGGAT
ENST00000376585.5:c.1875+52_1875+56delinsGGGAT	ENSP00000365770.1:n.1875+52_1875+56delinsGGGAT
ENST00000376590.7:c.1752+52_1752+56delinsGGGAT	ENSP00000365775.3:n.1752+52_1752+56delinsGGGAT
ENST00000376592.5:c.1752+52_1752+56delinsGGGAT	ENSP00000365777.1:n.1752+52_1752+56delinsGGGAT
NM_005957.4:c.1752+52_1752+56delinsGGGAT , LRG_726t1:c.1752+52_1752+56delinsGGGAT	NP_005948.3:n.1752+52_1752+56delinsGGGAT
XM_005263458.2:c.1875+52_1875+56delinsGGGAT	XP_005263515.1:n.1875+52_1875+56delinsGGGAT
XM_005263460.3:c.1752+52_1752+56delinsGGGAT	XP_005263517.1:n.1752+52_1752+56delinsGGGAT
XM_005263461.3:c.1752+52_1752+56delinsGGGAT	XP_005263518.1:n.1752+52_1752+56delinsGGGAT
XM_005263462.3:c.1752+52_1752+56delinsGGGAT	XP_005263519.1:n.1752+52_1752+56delinsGGGAT
XM_005263463.2:c.1506+52_1506+56delinsGGGAT	XP_005263520.1:n.1506+52_1506+56delinsGGGAT
XM_011541495.1:c.1872+52_1872+56delinsGGGAT	XP_011539797.1:n.1872+52_1872+56delinsGGGAT
XM_011541496.1:c.1875+52_1875+56delinsGGGAT	XP_011539798.1:n.1875+52_1875+56delinsGGGAT
NM_001330358.1:c.1875+52_1875+56delinsGGGAT	NP_001317287.1:n.1875+52_1875+56delinsGGGAT
XM_005263460.5:c.1752+52_1752+56delinsGGGAT	XP_005263517.1:n.1752+52_1752+56delinsGGGAT
XM_005263462.4:c.1752+52_1752+56delinsGGGAT	XP_005263519.1:n.1752+52_1752+56delinsGGGAT
XM_005263463.4:c.1506+52_1506+56delinsGGGAT	XP_005263520.1:n.1506+52_1506+56delinsGGGAT
XM_011541495.3:c.1872+52_1872+56delinsGGGAT	XP_011539797.1:n.1872+52_1872+56delinsGGGAT
XM_011541496.3:c.1875+52_1875+56delinsGGGAT	XP_011539798.1:n.1875+52_1875+56delinsGGGAT
XM_017001328.2:c.1875+52_1875+56delinsGGGAT	XP_016856817.1:n.1875+52_1875+56delinsGGGAT
XM_024447198.1:c.1506+52_1506+56delinsGGGAT	XP_024302966.1:n.1506+52_1506+56delinsGGGAT
XR_002956640.1:n.2853+52_2853+56delinsGGGAT
NM_005957.5:c.1752+52_1752+56delinsGGGAT MANE Select	NP_005948.3:n.1752+52_1752+56delinsGGGAT
NM_001330358.2:c.1875+52_1875+56delinsGGGAT	NP_001317287.1:n.1875+52_1875+56delinsGGGAT