Canonical Allele Identifier: CA1140625881
Gene: MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11801924_11801947delinsAAAAAAAAAAAAAAAAAAAAAAAA , CM000663.2:g.11801924_11801947delinsAAAAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000001.10:g.11861981_11862004delinsAAAAAAAAAAAAAAAAAAAAAAAA , CM000663.1:g.11861981_11862004delinsAAAAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000001.9:g.11784568_11784591delinsAAAAAAAAAAAAAAAAAAAAAAAA NCBI36
NG_008766.1:g.775_798delinsAAAAAAAAAAAAAAAAAAAAAAAA
NG_013351.1:g.9157_9180delinsTTTTTTTTTTTTTTTTTTTTTTTT , LRG_726:g.9157_9180delinsTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376486.3:c.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000365669.3:n.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTT...
ENST00000376585.6:c.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000365770.1:n.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTT...
ENST00000376590.9:c.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000365775.3:n.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTT...
ENST00000376592.6:c.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000365777.1:n.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTT...
ENST00000423400.7:c.357-548_357-525delinsTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000398908.3:n.357-548_357-525delinsTTTTTTTTTTTTTTTTTTTT...
ENST00000431243.6:n.1018-531_1018-508delinsTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000641407.1:c.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000493098.1:n.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTT...
ENST00000641437.1:n.369-548_369-525delinsTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000641446.1:c.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000493262.1:n.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTT...
ENST00000641721.1:n.294-548_294-525delinsTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000641747.1:c.236+934_236+957delinsTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000493116.1:n.236+934_236+957delinsTTTTTTTTTTTTTTTTTTTT...
ENST00000641759.1:n.372-548_372-525delinsTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000641805.1:n.520-548_520-525delinsTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000641909.1:n.647-548_647-525delinsTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000642002.1:n.466-531_466-508delinsTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000376583.7:c.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000365767.3:n.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTT...
ENST00000376585.5:c.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000365770.1:n.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTT...
ENST00000376590.7:c.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000365775.3:n.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTT...
ENST00000376592.5:c.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000365777.1:n.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTT...
ENST00000418034.1:c.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000405082.1:n.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTT...
NM_005957.4:c.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT , LRG_726t1:c.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT NP_005948.3:n.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT
XM_005263458.2:c.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTTTTTT XP_005263515.1:n.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTTTTT...
XM_005263460.3:c.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT XP_005263517.1:n.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTT...
XM_005263461.3:c.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT XP_005263518.1:n.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTT...
XM_005263462.3:c.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT XP_005263519.1:n.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTT...
XM_005263463.2:c.-27-531_-27-508delinsTTTTTTTTTTTTTTTTTTTTTTTT XP_005263520.1:n.-27-531_-27-508delinsTTTTTTTTTTTTTTTTTTTTTTT...
XM_011541495.1:c.357-548_357-525delinsTTTTTTTTTTTTTTTTTTTTTTTT XP_011539797.1:n.357-548_357-525delinsTTTTTTTTTTTTTTTTTTTTTTT...
XM_011541496.1:c.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTTTTTT XP_011539798.1:n.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTTTTT...
NM_001330358.1:c.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTTTTTT NP_001317287.1:n.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTTTTT...
XM_005263460.5:c.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT XP_005263517.1:n.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTT...
XM_005263462.4:c.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT XP_005263519.1:n.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTT...
XM_005263463.4:c.-27-531_-27-508delinsTTTTTTTTTTTTTTTTTTTTTTTT XP_005263520.1:n.-27-531_-27-508delinsTTTTTTTTTTTTTTTTTTTTTTT...
XM_011541495.3:c.357-548_357-525delinsTTTTTTTTTTTTTTTTTTTTTTTT XP_011539797.1:n.357-548_357-525delinsTTTTTTTTTTTTTTTTTTTTTTT...
XM_011541496.3:c.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTTTTTT XP_011539798.1:n.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTTTTT...
XM_017001328.2:c.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTTTTTT XP_016856817.1:n.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTTTTT...
XM_024447198.1:c.-27-531_-27-508delinsTTTTTTTTTTTTTTTTTTTTTTTT XP_024302966.1:n.-27-531_-27-508delinsTTTTTTTTTTTTTTTTTTTTTTT...
XR_002956640.1:n.1104-548_1104-525delinsTTTTTTTTTTTTTTTTTTTTTTTT
NM_005957.5:c.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_005948.3:n.237-548_237-525delinsTTTTTTTTTTTTTTTTTTTTTTTT
NM_001330358.2:c.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTTTTTT NP_001317287.1:n.360-548_360-525delinsTTTTTTTTTTTTTTTTTTTTTTT...