Canonical Allele Identifier: CA338422355
Gene: MTHFR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11801235C>G , CM000663.2:g.11801235C>G GRCh38
NC_000001.10:g.11861292C>G , CM000663.1:g.11861292C>G GRCh37
NC_000001.9:g.11783879C>G NCBI36
NG_008766.1:g.86C>G
NG_013351.1:g.9869G>C , LRG_726:g.9869G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376486.3:c.401G>C ENSP00000365669.3:p.Arg134Pro
ENST00000376585.6:c.524G>C ENSP00000365770.1:p.Arg175Pro
ENST00000376590.9:c.401G>C MANE Select ENSP00000365775.3:p.Arg134Pro
ENST00000376592.6:c.401G>C ENSP00000365777.1:p.Arg134Pro
ENST00000423400.7:c.521G>C ENSP00000398908.3:p.Arg174Pro
ENST00000641407.1:c.401G>C ENSP00000493098.1:p.Arg134Pro
ENST00000641437.1:n.533G>C
ENST00000641446.1:c.401G>C ENSP00000493262.1:p.Arg134Pro
ENST00000641721.1:n.458G>C
ENST00000641747.1:c.237-913G>C ENSP00000493116.1:n.237-913G>C
ENST00000641759.1:n.536G>C
ENST00000641805.1:n.684G>C
ENST00000641909.1:n.811G>C
ENST00000376583.7:c.524G>C ENSP00000365767.3:p.Arg175Pro
ENST00000376585.5:c.524G>C ENSP00000365770.1:p.Arg175Pro
ENST00000376590.7:c.401G>C ENSP00000365775.3:p.Arg134Pro
ENST00000376592.5:c.401G>C ENSP00000365777.1:p.Arg134Pro
ENST00000418034.1:c.401G>C ENSP00000405082.1:p.Arg134Pro
NM_005957.4:c.401G>C , LRG_726t1:c.401G>C NP_005948.3:p.Arg134Pro
XM_005263458.2:c.524G>C XP_005263515.1:p.Arg175Pro
XM_005263460.3:c.401G>C XP_005263517.1:p.Arg134Pro
XM_005263461.3:c.401G>C XP_005263518.1:p.Arg134Pro
XM_005263462.3:c.401G>C XP_005263519.1:p.Arg134Pro
XM_005263463.2:c.155G>C XP_005263520.1:p.Arg52Pro
XM_011541495.1:c.521G>C XP_011539797.1:p.Arg174Pro
XM_011541496.1:c.524G>C XP_011539798.1:p.Arg175Pro
NM_001330358.1:c.524G>C NP_001317287.1:p.Arg175Pro
XM_005263460.5:c.401G>C XP_005263517.1:p.Arg134Pro
XM_005263462.4:c.401G>C XP_005263519.1:p.Arg134Pro
XM_005263463.4:c.155G>C XP_005263520.1:p.Arg52Pro
XM_011541495.3:c.521G>C XP_011539797.1:p.Arg174Pro
XM_011541496.3:c.524G>C XP_011539798.1:p.Arg175Pro
XM_017001328.2:c.524G>C XP_016856817.1:p.Arg175Pro
XM_024447198.1:c.155G>C XP_024302966.1:p.Arg52Pro
XR_002956640.1:n.1268G>C
NM_005957.5:c.401G>C MANE Select NP_005948.3:p.Arg134Pro
NM_001330358.2:c.524G>C NP_001317287.1:p.Arg175Pro