Canonical Allele Identifier: CA1153791480
Gene: MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11790900_11790920delinsTACACACACATACCCCCGCAC , CM000663.2:g.11790900_11790920delinsTACACACACATACCCCCGCAC GRCh38
NC_000001.10:g.11850957_11850977delinsTACACACACATACCCCCGCAC , CM000663.1:g.11850957_11850977delinsTACACACACATACCCCCGCAC GRCh37
NC_000001.9:g.11773544_11773564delinsTACACACACATACCCCCGCAC NCBI36
NG_013351.1:g.20184_20204delinsGTGCGGGGGTATGTGTGTGTA , LRG_726:g.20184_20204delinsGTGCGGGGGTATGTGTGTGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376585.6:c.1876-22_1876-2delinsGTGCGGGGGTATGTGTGTGTA ENSP00000365770.1:n.1876-22_1876-2delinsGTGCGGGGGTATGTGTGTGTA...
ENST00000376590.9:c.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA MANE Select ENSP00000365775.3:n.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA...
ENST00000376592.6:c.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA ENSP00000365777.1:n.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA...
ENST00000423400.7:c.1873-22_1873-2delinsGTGCGGGGGTATGTGTGTGTA ENSP00000398908.3:n.1873-22_1873-2delinsGTGCGGGGGTATGTGTGTGTA...
ENST00000641407.1:c.1753-204_1753-184delinsGTGCGGGGGTATGTGTGTGTA ENSP00000493098.1:n.1753-204_1753-184delinsGTGCGGGGGTATGTGTGT...
ENST00000641446.1:c.*212-22_*212-2delinsGTGCGGGGGTATGTGTGTGTA ENSP00000493262.1:n.*212-22_*212-2delinsGTGCGGGGGTATGTGTGTGTA...
ENST00000641747.1:c.*1265-22_*1265-2delinsGTGCGGGGGTATGTGTGTGTA ENSP00000493116.1:n.*1265-22_*1265-2delinsGTGCGGGGGTATGTGTGTG...
ENST00000641759.1:n.2122-22_2122-2delinsGTGCGGGGGTATGTGTGTGTA
ENST00000641805.1:n.2270-204_2270-184delinsGTGCGGGGGTATGTGTGTGTA
ENST00000641820.1:c.1018-22_1018-2delinsGTGCGGGGGTATGTGTGTGTA ENSP00000492937.1:n.1018-22_1018-2delinsGTGCGGGGGTATGTGTGTGTA...
ENST00000376583.7:c.1876-22_1876-2delinsGTGCGGGGGTATGTGTGTGTA ENSP00000365767.3:n.1876-22_1876-2delinsGTGCGGGGGTATGTGTGTGTA...
ENST00000376585.5:c.1876-22_1876-2delinsGTGCGGGGGTATGTGTGTGTA ENSP00000365770.1:n.1876-22_1876-2delinsGTGCGGGGGTATGTGTGTGTA...
ENST00000376590.7:c.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA ENSP00000365775.3:n.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA...
ENST00000376592.5:c.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA ENSP00000365777.1:n.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA...
NM_005957.4:c.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA , LRG_726t1:c.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA NP_005948.3:n.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA
XM_005263458.2:c.1876-22_1876-2delinsGTGCGGGGGTATGTGTGTGTA XP_005263515.1:n.1876-22_1876-2delinsGTGCGGGGGTATGTGTGTGTA
XM_005263460.3:c.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA XP_005263517.1:n.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA
XM_005263461.3:c.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA XP_005263518.1:n.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA
XM_005263462.3:c.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA XP_005263519.1:n.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA
XM_005263463.2:c.1507-22_1507-2delinsGTGCGGGGGTATGTGTGTGTA XP_005263520.1:n.1507-22_1507-2delinsGTGCGGGGGTATGTGTGTGTA
XM_011541495.1:c.1873-22_1873-2delinsGTGCGGGGGTATGTGTGTGTA XP_011539797.1:n.1873-22_1873-2delinsGTGCGGGGGTATGTGTGTGTA
XM_011541496.1:c.1876-204_1876-184delinsGTGCGGGGGTATGTGTGTGTA XP_011539798.1:n.1876-204_1876-184delinsGTGCGGGGGTATGTGTGTGTA...
NM_001330358.1:c.1876-22_1876-2delinsGTGCGGGGGTATGTGTGTGTA NP_001317287.1:n.1876-22_1876-2delinsGTGCGGGGGTATGTGTGTGTA
XM_005263460.5:c.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA XP_005263517.1:n.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA
XM_005263462.4:c.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA XP_005263519.1:n.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA
XM_005263463.4:c.1507-22_1507-2delinsGTGCGGGGGTATGTGTGTGTA XP_005263520.1:n.1507-22_1507-2delinsGTGCGGGGGTATGTGTGTGTA
XM_011541495.3:c.1873-22_1873-2delinsGTGCGGGGGTATGTGTGTGTA XP_011539797.1:n.1873-22_1873-2delinsGTGCGGGGGTATGTGTGTGTA
XM_011541496.3:c.1876-204_1876-184delinsGTGCGGGGGTATGTGTGTGTA XP_011539798.1:n.1876-204_1876-184delinsGTGCGGGGGTATGTGTGTGTA...
XM_017001328.2:c.1876-172_1876-152delinsGTGCGGGGGTATGTGTGTGTA XP_016856817.1:n.1876-172_1876-152delinsGTGCGGGGGTATGTGTGTGTA...
XM_024447198.1:c.1507-22_1507-2delinsGTGCGGGGGTATGTGTGTGTA XP_024302966.1:n.1507-22_1507-2delinsGTGCGGGGGTATGTGTGTGTA
XR_002956640.1:n.2854-204_2854-184delinsGTGCGGGGGTATGTGTGTGTA
NM_005957.5:c.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA MANE Select NP_005948.3:n.1753-22_1753-2delinsGTGCGGGGGTATGTGTGTGTA
NM_001330358.2:c.1876-22_1876-2delinsGTGCGGGGGTATGTGTGTGTA NP_001317287.1:n.1876-22_1876-2delinsGTGCGGGGGTATGTGTGTGTA