Canonical Allele Identifier: CA1153811593
Gene: MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11800625_11800626delinsAT , CM000663.2:g.11800625_11800626delinsAT GRCh38
NC_000001.10:g.11860682_11860683delinsAT , CM000663.1:g.11860682_11860683delinsAT GRCh37
NC_000001.9:g.11783269_11783270delinsAT NCBI36
NG_013351.1:g.10478_10479delinsAT , LRG_726:g.10478_10479delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000376486.3:c.476-304_476-303delinsAT ENSP00000365669.3:n.476-304_476-303delins...
ENST00000376585.6:c.599-304_599-303delinsAT ENSP00000365770.1:n.599-304_599-303delins...
ENST00000376590.9:c.476-304_476-303delinsAT MANE Select ENSP00000365775.3:n.476-304_476-303delins...
ENST00000376592.6:c.476-304_476-303delinsAT ENSP00000365777.1:n.476-304_476-303delins...
ENST00000423400.7:c.596-304_596-303delinsAT ENSP00000398908.3:n.596-304_596-303delins...
ENST00000641407.1:c.476-304_476-303delinsAT ENSP00000493098.1:n.476-304_476-303delins...
ENST00000641437.1:n.1142_1143delinsAT
ENST00000641446.1:c.476-304_476-303delinsAT ENSP00000493262.1:n.476-304_476-303delins...
ENST00000641721.1:n.533-304_533-303delinsAT
ENST00000641747.1:c.237-304_237-303delinsAT ENSP00000493116.1:n.237-304_237-303delins...
ENST00000641759.1:n.611-304_611-303delinsAT
ENST00000641805.1:n.759-304_759-303delinsAT
ENST00000641909.1:n.1420_1421delinsAT
ENST00000376583.7:c.599-304_599-303delinsAT ENSP00000365767.3:n.599-304_599-303delins...
ENST00000376585.5:c.599-304_599-303delinsAT ENSP00000365770.1:n.599-304_599-303delins...
ENST00000376590.7:c.476-304_476-303delinsAT ENSP00000365775.3:n.476-304_476-303delins...
ENST00000376592.5:c.476-304_476-303delinsAT ENSP00000365777.1:n.476-304_476-303delins...
NM_005957.4:c.476-304_476-303delinsAT , LRG_726t1:c.476-304_476-303delinsAT NP_005948.3:n.476-304_476-303delinsAT
XM_005263458.2:c.599-304_599-303delinsAT XP_005263515.1:n.599-304_599-303delinsAT
XM_005263460.3:c.476-304_476-303delinsAT XP_005263517.1:n.476-304_476-303delinsAT
XM_005263461.3:c.476-304_476-303delinsAT XP_005263518.1:n.476-304_476-303delinsAT
XM_005263462.3:c.476-304_476-303delinsAT XP_005263519.1:n.476-304_476-303delinsAT
XM_005263463.2:c.230-304_230-303delinsAT XP_005263520.1:n.230-304_230-303delinsAT
XM_011541495.1:c.596-304_596-303delinsAT XP_011539797.1:n.596-304_596-303delinsAT
XM_011541496.1:c.599-304_599-303delinsAT XP_011539798.1:n.599-304_599-303delinsAT
NM_001330358.1:c.599-304_599-303delinsAT NP_001317287.1:n.599-304_599-303delinsAT
XM_005263460.5:c.476-304_476-303delinsAT XP_005263517.1:n.476-304_476-303delinsAT
XM_005263462.4:c.476-304_476-303delinsAT XP_005263519.1:n.476-304_476-303delinsAT
XM_005263463.4:c.230-304_230-303delinsAT XP_005263520.1:n.230-304_230-303delinsAT
XM_011541495.3:c.596-304_596-303delinsAT XP_011539797.1:n.596-304_596-303delinsAT
XM_011541496.3:c.599-304_599-303delinsAT XP_011539798.1:n.599-304_599-303delinsAT
XM_017001328.2:c.599-304_599-303delinsAT XP_016856817.1:n.599-304_599-303delinsAT
XM_024447198.1:c.230-304_230-303delinsAT XP_024302966.1:n.230-304_230-303delinsAT
XR_002956640.1:n.1343-304_1343-303delinsAT
NM_005957.5:c.476-304_476-303delinsAT MANE Select NP_005948.3:n.476-304_476-303delinsAT
NM_001330358.2:c.599-304_599-303delinsAT NP_001317287.1:n.599-304_599-303delinsAT