Canonical Allele Identifier: CA1153810324
Gene: MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11803274T= , CM000663.2:g.11803274T= GRCh38
NC_000001.10:g.11863331T= , CM000663.1:g.11863331T= GRCh37
NC_000001.9:g.11785918T= NCBI36
NG_008766.1:g.2125T=
NG_013351.1:g.7830A= , LRG_726:g.7830A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376486.3:c.-10-148A= ENSP00000365669.3:n.-10-148A=
ENST00000376585.6:c.110+131A= ENSP00000365770.1:n.110+131A=
ENST00000376590.9:c.-13-145A= MANE Select ENSP00000365775.3:n.-13-145A=
ENST00000376592.6:c.-158A= ENSP00000365777.1:n.-158A=
ENST00000423400.7:c.110+131A= ENSP00000398908.3:n.110+131A=
ENST00000431243.6:n.769-145A=
ENST00000641407.1:c.-158A= ENSP00000493098.1:n.-158A=
ENST00000641437.1:n.120-145A=
ENST00000641446.1:c.-13-145A= ENSP00000493262.1:n.-13-145A=
ENST00000641721.1:n.44+131A=
ENST00000641747.1:c.-13-145A= ENSP00000493116.1:n.-13-145A=
ENST00000641759.1:n.122+131A=
ENST00000641805.1:n.273+131A=
ENST00000641909.1:n.253A=
ENST00000642002.1:n.217-145A=
ENST00000376486.2:c.-13-145A= ENSP00000365669.2:n.-13-145A=
ENST00000376583.7:c.110+131A= ENSP00000365767.3:n.110+131A=
ENST00000376585.5:c.110+131A= ENSP00000365770.1:n.110+131A=
ENST00000376590.7:c.-13-145A= ENSP00000365775.3:n.-13-145A=
ENST00000413656.5:c.-13-145A= ENSP00000408307.1:n.-13-145A=
ENST00000418034.1:c.-13-145A= ENSP00000405082.1:n.-13-145A=
ENST00000423400.5:c.-89A= ENSP00000398908.1:n.-89A=
ENST00000431243.5:c.-13-145A= ENSP00000400460.1:n.-13-145A=
NM_005957.4:c.-13-145A= , LRG_726t1:c.-13-145A= NP_005948.3:n.-13-145A=
XM_005263458.2:c.110+131A= XP_005263515.1:n.110+131A=
XM_005263460.3:c.-13-145A= XP_005263517.1:n.-13-145A=
XM_005263461.3:c.-10-148A= XP_005263518.1:n.-10-148A=
XM_005263462.3:c.-10-148A= XP_005263519.1:n.-10-148A=
XM_005263463.2:c.-276-145A= XP_005263520.1:n.-276-145A=
XM_011541495.1:c.110+131A= XP_011539797.1:n.110+131A=
XM_011541496.1:c.110+131A= XP_011539798.1:n.110+131A=
NM_001330358.1:c.110+131A= NP_001317287.1:n.110+131A=
XM_005263460.5:c.-13-145A= XP_005263517.1:n.-13-145A=
XM_005263462.4:c.-10-148A= XP_005263519.1:n.-10-148A=
XM_005263463.4:c.-276-145A= XP_005263520.1:n.-276-145A=
XM_011541495.3:c.110+131A= XP_011539797.1:n.110+131A=
XM_011541496.3:c.110+131A= XP_011539798.1:n.110+131A=
XM_017001328.2:c.110+131A= XP_016856817.1:n.110+131A=
XM_024447198.1:c.-277+131A= XP_024302966.1:n.-277+131A=
XR_002956640.1:n.857+131A=
NM_005957.5:c.-13-145A= MANE Select NP_005948.3:n.-13-145A=
NM_001330358.2:c.110+131A= NP_001317287.1:n.110+131A=