Canonical Allele Identifier: CA2831039343
Gene: MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11802919del , CM000663.2:g.11802919del GRCh38
NC_000001.10:g.11862976del , CM000663.1:g.11862976del GRCh37
NC_000001.9:g.11785563del NCBI36
NG_008766.1:g.1770del
NG_013351.1:g.8185del , LRG_726:g.8185del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376486.3:c.198del ENSP00000365669.3:p.Pro67LeufsTer25
ENST00000376585.6:c.321del ENSP00000365770.1:p.Pro108LeufsTer25
ENST00000376590.9:c.198del MANE Select ENSP00000365775.3:p.Pro67LeufsTer25
ENST00000376592.6:c.198del ENSP00000365777.1:p.Pro67LeufsTer25
ENST00000423400.7:c.318del ENSP00000398908.3:p.Pro107LeufsTer25
ENST00000431243.6:n.979del
ENST00000641407.1:c.198del ENSP00000493098.1:p.Pro67LeufsTer25
ENST00000641437.1:n.330del
ENST00000641446.1:c.198del ENSP00000493262.1:p.Pro67LeufsTer25
ENST00000641721.1:n.255del
ENST00000641747.1:c.198del ENSP00000493116.1:p.Pro67LeufsTer?
ENST00000641759.1:n.333del
ENST00000641805.1:n.481del
ENST00000641909.1:n.608del
ENST00000642002.1:n.427del
ENST00000376583.7:c.321del ENSP00000365767.3:p.Pro108LeufsTer25
ENST00000376585.5:c.321del ENSP00000365770.1:p.Pro108LeufsTer25
ENST00000376590.7:c.198del ENSP00000365775.3:p.Pro67LeufsTer25
ENST00000376592.5:c.198del ENSP00000365777.1:p.Pro67LeufsTer25
ENST00000418034.1:c.198del ENSP00000405082.1:p.Pro67LeufsTer25
NM_005957.4:c.198del , LRG_726t1:c.198del NP_005948.3:p.Pro67LeufsTer25
XM_005263458.2:c.321del XP_005263515.1:p.Pro108LeufsTer25
XM_005263460.3:c.198del XP_005263517.1:p.Pro67LeufsTer25
XM_005263461.3:c.198del XP_005263518.1:p.Pro67LeufsTer25
XM_005263462.3:c.198del XP_005263519.1:p.Pro67LeufsTer25
XM_005263463.2:c.-66del XP_005263520.1:n.-66del
XM_011541495.1:c.318del XP_011539797.1:p.Pro107LeufsTer25
XM_011541496.1:c.321del XP_011539798.1:p.Pro108LeufsTer25
NM_001330358.1:c.321del NP_001317287.1:p.Pro108LeufsTer25
XM_005263460.5:c.198del XP_005263517.1:p.Pro67LeufsTer25
XM_005263462.4:c.198del XP_005263519.1:p.Pro67LeufsTer25
XM_005263463.4:c.-66del XP_005263520.1:n.-66del
XM_011541495.3:c.318del XP_011539797.1:p.Pro107LeufsTer25
XM_011541496.3:c.321del XP_011539798.1:p.Pro108LeufsTer25
XM_017001328.2:c.321del XP_016856817.1:p.Pro108LeufsTer25
XM_024447198.1:c.-66del XP_024302966.1:n.-66del
XR_002956640.1:n.1065del
NM_005957.5:c.198del MANE Select NP_005948.3:p.Pro67LeufsTer25
NM_001330358.2:c.321del NP_001317287.1:p.Pro108LeufsTer25