Canonical Allele Identifier: CA1153799286
Gene: MTHFR HGNC NCBI

Linked Data

dbSNP Id: rs1644206007

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11794555_11794556insCTCTG , CM000663.2:g.11794555_11794556insCTCTG GRCh38
NC_000001.10:g.11854612_11854613insCTCTG , CM000663.1:g.11854612_11854613insCTCTG GRCh37
NC_000001.9:g.11777199_11777200insCTCTG NCBI36
NG_013351.1:g.16548_16549insCAGAG , LRG_726:g.16548_16549insCAGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376585.6:c.1290-18_1290-17insCAGAG ENSP00000365770.1:n.1290-18_1290-17insCAGAG
ENST00000376590.9:c.1167-18_1167-17insCAGAG MANE Select ENSP00000365775.3:n.1167-18_1167-17insCAGAG
ENST00000376592.6:c.1167-18_1167-17insCAGAG ENSP00000365777.1:n.1167-18_1167-17insCAGAG
ENST00000423400.7:c.1287-18_1287-17insCAGAG ENSP00000398908.3:n.1287-18_1287-17insCAGAG
ENST00000641407.1:c.1167-18_1167-17insCAGAG ENSP00000493098.1:n.1167-18_1167-17insCAGAG
ENST00000641446.1:c.1167-18_1167-17insCAGAG ENSP00000493262.1:n.1167-18_1167-17insCAGAG
ENST00000641747.1:c.*679-18_*679-17insCAGAG ENSP00000493116.1:n.*679-18_*679-17insCAGAG
ENST00000641759.1:n.1536-18_1536-17insCAGAG
ENST00000641805.1:n.1684-18_1684-17insCAGAG
ENST00000641820.1:c.432-18_432-17insCAGAG ENSP00000492937.1:n.432-18_432-17insCAGAG
ENST00000376583.7:c.1290-18_1290-17insCAGAG ENSP00000365767.3:n.1290-18_1290-17insCAGAG
ENST00000376585.5:c.1290-18_1290-17insCAGAG ENSP00000365770.1:n.1290-18_1290-17insCAGAG
ENST00000376590.7:c.1167-18_1167-17insCAGAG ENSP00000365775.3:n.1167-18_1167-17insCAGAG
ENST00000376592.5:c.1167-18_1167-17insCAGAG ENSP00000365777.1:n.1167-18_1167-17insCAGAG
NM_005957.4:c.1167-18_1167-17insCAGAG , LRG_726t1:c.1167-18_1167-17insCAGAG NP_005948.3:n.1167-18_1167-17insCAGAG
XM_005263458.2:c.1290-18_1290-17insCAGAG XP_005263515.1:n.1290-18_1290-17insCAGAG
XM_005263460.3:c.1167-18_1167-17insCAGAG XP_005263517.1:n.1167-18_1167-17insCAGAG
XM_005263461.3:c.1167-18_1167-17insCAGAG XP_005263518.1:n.1167-18_1167-17insCAGAG
XM_005263462.3:c.1167-18_1167-17insCAGAG XP_005263519.1:n.1167-18_1167-17insCAGAG
XM_005263463.2:c.921-18_921-17insCAGAG XP_005263520.1:n.921-18_921-17insCAGAG
XM_011541495.1:c.1287-18_1287-17insCAGAG XP_011539797.1:n.1287-18_1287-17insCAGAG
XM_011541496.1:c.1290-18_1290-17insCAGAG XP_011539798.1:n.1290-18_1290-17insCAGAG
NM_001330358.1:c.1290-18_1290-17insCAGAG NP_001317287.1:n.1290-18_1290-17insCAGAG
XM_005263460.5:c.1167-18_1167-17insCAGAG XP_005263517.1:n.1167-18_1167-17insCAGAG
XM_005263462.4:c.1167-18_1167-17insCAGAG XP_005263519.1:n.1167-18_1167-17insCAGAG
XM_005263463.4:c.921-18_921-17insCAGAG XP_005263520.1:n.921-18_921-17insCAGAG
XM_011541495.3:c.1287-18_1287-17insCAGAG XP_011539797.1:n.1287-18_1287-17insCAGAG
XM_011541496.3:c.1290-18_1290-17insCAGAG XP_011539798.1:n.1290-18_1290-17insCAGAG
XM_017001328.2:c.1290-18_1290-17insCAGAG XP_016856817.1:n.1290-18_1290-17insCAGAG
XM_024447198.1:c.921-18_921-17insCAGAG XP_024302966.1:n.921-18_921-17insCAGAG
XR_002956640.1:n.2268-18_2268-17insCAGAG
NM_005957.5:c.1167-18_1167-17insCAGAG MANE Select NP_005948.3:n.1167-18_1167-17insCAGAG
NM_001330358.2:c.1290-18_1290-17insCAGAG NP_001317287.1:n.1290-18_1290-17insCAGAG