Canonical Allele Identifier: CA2643302841
Gene: MTHFR HGNC NCBI

Linked Data

gnomAD v4: 1-11791394-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11791394C>A , CM000663.2:g.11791394C>A GRCh38
NC_000001.10:g.11851451C>A , CM000663.1:g.11851451C>A GRCh37
NC_000001.9:g.11774038C>A NCBI36
NG_013351.1:g.19710G>T , LRG_726:g.19710G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376585.6:c.1756-68G>T ENSP00000365770.1:n.1756-68G>T
ENST00000376590.9:c.1633-68G>T MANE Select ENSP00000365775.3:n.1633-68G>T
ENST00000376592.6:c.1633-68G>T ENSP00000365777.1:n.1633-68G>T
ENST00000423400.7:c.1753-68G>T ENSP00000398908.3:n.1753-68G>T
ENST00000641407.1:c.1633-68G>T ENSP00000493098.1:n.1633-68G>T
ENST00000641446.1:c.*92-68G>T ENSP00000493262.1:n.*92-68G>T
ENST00000641747.1:c.*1145-68G>T ENSP00000493116.1:n.*1145-68G>T
ENST00000641759.1:n.2002-68G>T
ENST00000641805.1:n.2150-68G>T
ENST00000641820.1:c.898-68G>T ENSP00000492937.1:n.898-68G>T
ENST00000376583.7:c.1756-68G>T ENSP00000365767.3:n.1756-68G>T
ENST00000376585.5:c.1756-68G>T ENSP00000365770.1:n.1756-68G>T
ENST00000376590.7:c.1633-68G>T ENSP00000365775.3:n.1633-68G>T
ENST00000376592.5:c.1633-68G>T ENSP00000365777.1:n.1633-68G>T
NM_005957.4:c.1633-68G>T , LRG_726t1:c.1633-68G>T NP_005948.3:n.1633-68G>T
XM_005263458.2:c.1756-68G>T XP_005263515.1:n.1756-68G>T
XM_005263460.3:c.1633-68G>T XP_005263517.1:n.1633-68G>T
XM_005263461.3:c.1633-68G>T XP_005263518.1:n.1633-68G>T
XM_005263462.3:c.1633-68G>T XP_005263519.1:n.1633-68G>T
XM_005263463.2:c.1387-68G>T XP_005263520.1:n.1387-68G>T
XM_011541495.1:c.1753-68G>T XP_011539797.1:n.1753-68G>T
XM_011541496.1:c.1756-68G>T XP_011539798.1:n.1756-68G>T
NM_001330358.1:c.1756-68G>T NP_001317287.1:n.1756-68G>T
XM_005263460.5:c.1633-68G>T XP_005263517.1:n.1633-68G>T
XM_005263462.4:c.1633-68G>T XP_005263519.1:n.1633-68G>T
XM_005263463.4:c.1387-68G>T XP_005263520.1:n.1387-68G>T
XM_011541495.3:c.1753-68G>T XP_011539797.1:n.1753-68G>T
XM_011541496.3:c.1756-68G>T XP_011539798.1:n.1756-68G>T
XM_017001328.2:c.1756-68G>T XP_016856817.1:n.1756-68G>T
XM_024447198.1:c.1387-68G>T XP_024302966.1:n.1387-68G>T
XR_002956640.1:n.2734-68G>T
NM_005957.5:c.1633-68G>T MANE Select NP_005948.3:n.1633-68G>T
NM_001330358.2:c.1756-68G>T NP_001317287.1:n.1756-68G>T