Canonical Allele Identifier: CA2643298995
Gene: MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11790271_11790309del , CM000663.2:g.11790271_11790309del GRCh38
NC_000001.10:g.11850328_11850366del , CM000663.1:g.11850328_11850366del GRCh37
NC_000001.9:g.11772915_11772953del NCBI36
NG_013351.1:g.20797_20835del , LRG_726:g.20797_20835del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376585.6:c.*373_*411del ENSP00000365770.1:n.*373_*411del
ENST00000376590.9:c.*373_*411del MANE Select ENSP00000365775.3:n.*373_*411del
ENST00000376592.6:c.*373_*411del ENSP00000365777.1:n.*373_*411del
ENST00000423400.7:c.*373_*411del ENSP00000398908.3:n.*373_*411del
ENST00000641446.1:c.*803_*841del ENSP00000493262.1:n.*803_*841del
ENST00000641747.1:c.*1856_*1894del ENSP00000493116.1:n.*1856_*1894del
ENST00000641805.1:n.2679_2717del
ENST00000376583.7:c.2467_2505del ENSP00000365767.3:n.2467_2505del
ENST00000376585.5:c.*373_*411del ENSP00000365770.1:n.*373_*411del
ENST00000376590.7:c.*373_*411del ENSP00000365775.3:n.*373_*411del
ENST00000376592.5:c.*373_*411del ENSP00000365777.1:n.*373_*411del
NM_005957.4:c.*373_*411del , LRG_726t1:c.*373_*411del NP_005948.3:n.*373_*411del
XM_005263458.2:c.*373_*411del XP_005263515.1:n.*373_*411del
XM_005263460.3:c.*373_*411del XP_005263517.1:n.*373_*411del
XM_005263461.3:c.*373_*411del XP_005263518.1:n.*373_*411del
XM_005263462.3:c.*373_*411del XP_005263519.1:n.*373_*411del
XM_005263463.2:c.*373_*411del XP_005263520.1:n.*373_*411del
XM_011541495.1:c.*373_*411del XP_011539797.1:n.*373_*411del
XM_011541496.1:c.*233_*271del XP_011539798.1:n.*233_*271del
NM_001330358.1:c.*373_*411del NP_001317287.1:n.*373_*411del
XM_005263460.5:c.*373_*411del XP_005263517.1:n.*373_*411del
XM_005263462.4:c.*373_*411del XP_005263519.1:n.*373_*411del
XM_005263463.4:c.*373_*411del XP_005263520.1:n.*373_*411del
XM_011541495.3:c.*373_*411del XP_011539797.1:n.*373_*411del
XM_011541496.3:c.*233_*271del XP_011539798.1:n.*233_*271del
XM_024447198.1:c.*373_*411del XP_024302966.1:n.*373_*411del
NM_005957.5:c.*373_*411del MANE Select NP_005948.3:n.*373_*411del
NM_001330358.2:c.*373_*411del NP_001317287.1:n.*373_*411del