Canonical Allele Identifier: CA1153792097

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11791103_11791104delinsAG , CM000663.2:g.11791103_11791104delinsAG	GRCh38
NC_000001.10:g.11851160_11851161delinsAG , CM000663.1:g.11851160_11851161delinsAG	GRCh37
NC_000001.9:g.11773747_11773748delinsAG	NCBI36
NG_013351.1:g.20000_20001delinsCT , LRG_726:g.20000_20001delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.1875+103_1875+104delinsCT	ENSP00000365770.1:n.1875+103_1875+104delinsCT
ENST00000376590.9:c.1752+103_1752+104delinsCT MANE Select	ENSP00000365775.3:n.1752+103_1752+104delinsCT
ENST00000376592.6:c.1752+103_1752+104delinsCT	ENSP00000365777.1:n.1752+103_1752+104delinsCT
ENST00000423400.7:c.1872+103_1872+104delinsCT	ENSP00000398908.3:n.1872+103_1872+104delinsCT
ENST00000641407.1:c.1752+103_1752+104delinsCT	ENSP00000493098.1:n.1752+103_1752+104delinsCT
ENST00000641446.1:c.*211+103_*211+104delinsCT	ENSP00000493262.1:n.*211+103_*211+104delinsCT
ENST00000641747.1:c.*1264+103_*1264+104delinsCT	ENSP00000493116.1:n.*1264+103_*1264+104delinsCT
ENST00000641759.1:n.2121+103_2121+104delinsCT
ENST00000641805.1:n.2269+103_2269+104delinsCT
ENST00000641820.1:c.1017+103_1017+104delinsCT	ENSP00000492937.1:n.1017+103_1017+104delinsCT
ENST00000376583.7:c.1875+103_1875+104delinsCT	ENSP00000365767.3:n.1875+103_1875+104delinsCT
ENST00000376585.5:c.1875+103_1875+104delinsCT	ENSP00000365770.1:n.1875+103_1875+104delinsCT
ENST00000376590.7:c.1752+103_1752+104delinsCT	ENSP00000365775.3:n.1752+103_1752+104delinsCT
ENST00000376592.5:c.1752+103_1752+104delinsCT	ENSP00000365777.1:n.1752+103_1752+104delinsCT
NM_005957.4:c.1752+103_1752+104delinsCT , LRG_726t1:c.1752+103_1752+104delinsCT	NP_005948.3:n.1752+103_1752+104delinsCT
XM_005263458.2:c.1875+103_1875+104delinsCT	XP_005263515.1:n.1875+103_1875+104delinsCT
XM_005263460.3:c.1752+103_1752+104delinsCT	XP_005263517.1:n.1752+103_1752+104delinsCT
XM_005263461.3:c.1752+103_1752+104delinsCT	XP_005263518.1:n.1752+103_1752+104delinsCT
XM_005263462.3:c.1752+103_1752+104delinsCT	XP_005263519.1:n.1752+103_1752+104delinsCT
XM_005263463.2:c.1506+103_1506+104delinsCT	XP_005263520.1:n.1506+103_1506+104delinsCT
XM_011541495.1:c.1872+103_1872+104delinsCT	XP_011539797.1:n.1872+103_1872+104delinsCT
XM_011541496.1:c.1875+103_1875+104delinsCT	XP_011539798.1:n.1875+103_1875+104delinsCT
NM_001330358.1:c.1875+103_1875+104delinsCT	NP_001317287.1:n.1875+103_1875+104delinsCT
XM_005263460.5:c.1752+103_1752+104delinsCT	XP_005263517.1:n.1752+103_1752+104delinsCT
XM_005263462.4:c.1752+103_1752+104delinsCT	XP_005263519.1:n.1752+103_1752+104delinsCT
XM_005263463.4:c.1506+103_1506+104delinsCT	XP_005263520.1:n.1506+103_1506+104delinsCT
XM_011541495.3:c.1872+103_1872+104delinsCT	XP_011539797.1:n.1872+103_1872+104delinsCT
XM_011541496.3:c.1875+103_1875+104delinsCT	XP_011539798.1:n.1875+103_1875+104delinsCT
XM_017001328.2:c.1875+103_1875+104delinsCT	XP_016856817.1:n.1875+103_1875+104delinsCT
XM_024447198.1:c.1506+103_1506+104delinsCT	XP_024302966.1:n.1506+103_1506+104delinsCT
XR_002956640.1:n.2853+103_2853+104delinsCT
NM_005957.5:c.1752+103_1752+104delinsCT MANE Select	NP_005948.3:n.1752+103_1752+104delinsCT
NM_001330358.2:c.1875+103_1875+104delinsCT	NP_001317287.1:n.1875+103_1875+104delinsCT