Canonical Allele Identifier: CA2574214309
Gene: MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11795035del , CM000663.2:g.11795035del GRCh38
NC_000001.10:g.11855092del , CM000663.1:g.11855092del GRCh37
NC_000001.9:g.11777679del NCBI36
NG_013351.1:g.16070del , LRG_726:g.16070del

Transcript Alleles

HGVS Amino-acid change
ENST00000376585.6:c.1154+64del ENSP00000365770.1:n.1154+64del
ENST00000376590.9:c.1031+64del MANE Select ENSP00000365775.3:n.1031+64del
ENST00000376592.6:c.1031+64del ENSP00000365777.1:n.1031+64del
ENST00000423400.7:c.1151+64del ENSP00000398908.3:n.1151+64del
ENST00000641407.1:c.1031+64del ENSP00000493098.1:n.1031+64del
ENST00000641446.1:c.1031+64del ENSP00000493262.1:n.1031+64del
ENST00000641747.1:c.*543+64del ENSP00000493116.1:n.*543+64del
ENST00000641759.1:n.1230del
ENST00000641805.1:n.1378del
ENST00000641820.1:c.296+64del ENSP00000492937.1:n.296+64del
ENST00000376583.7:c.1154+64del ENSP00000365767.3:n.1154+64del
ENST00000376585.5:c.1154+64del ENSP00000365770.1:n.1154+64del
ENST00000376590.7:c.1031+64del ENSP00000365775.3:n.1031+64del
ENST00000376592.5:c.1031+64del ENSP00000365777.1:n.1031+64del
NM_005957.4:c.1031+64del , LRG_726t1:c.1031+64del NP_005948.3:n.1031+64del
XM_005263458.2:c.1154+64del XP_005263515.1:n.1154+64del
XM_005263460.3:c.1031+64del XP_005263517.1:n.1031+64del
XM_005263461.3:c.1031+64del XP_005263518.1:n.1031+64del
XM_005263462.3:c.1031+64del XP_005263519.1:n.1031+64del
XM_005263463.2:c.785+64del XP_005263520.1:n.785+64del
XM_011541495.1:c.1151+64del XP_011539797.1:n.1151+64del
XM_011541496.1:c.1154+64del XP_011539798.1:n.1154+64del
NM_001330358.1:c.1154+64del NP_001317287.1:n.1154+64del
XM_005263460.5:c.1031+64del XP_005263517.1:n.1031+64del
XM_005263462.4:c.1031+64del XP_005263519.1:n.1031+64del
XM_005263463.4:c.785+64del XP_005263520.1:n.785+64del
XM_011541495.3:c.1151+64del XP_011539797.1:n.1151+64del
XM_011541496.3:c.1154+64del XP_011539798.1:n.1154+64del
XM_017001328.2:c.1154+64del XP_016856817.1:n.1154+64del
XM_024447198.1:c.785+64del XP_024302966.1:n.785+64del
XR_002956640.1:n.1962del
NM_005957.5:c.1031+64del MANE Select NP_005948.3:n.1031+64del
NM_001330358.2:c.1154+64del NP_001317287.1:n.1154+64del