Canonical Allele Identifier: CA1153802688

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11795979_11795980delinsCA , CM000663.2:g.11795979_11795980delinsCA	GRCh38
NC_000001.10:g.11856036_11856037delinsCA , CM000663.1:g.11856036_11856037delinsCA	GRCh37
NC_000001.9:g.11778623_11778624delinsCA	NCBI36
NG_013351.1:g.15124_15125delinsTG , LRG_726:g.15124_15125delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.903+226_903+227delinsTG	ENSP00000365770.1:n.903+226_903+227delinsTG
ENST00000376590.9:c.780+226_780+227delinsTG MANE Select	ENSP00000365775.3:n.780+226_780+227delinsTG
ENST00000376592.6:c.780+226_780+227delinsTG	ENSP00000365777.1:n.780+226_780+227delinsTG
ENST00000423400.7:c.900+226_900+227delinsTG	ENSP00000398908.3:n.900+226_900+227delinsTG
ENST00000641407.1:c.780+226_780+227delinsTG	ENSP00000493098.1:n.780+226_780+227delinsTG
ENST00000641446.1:c.780+226_780+227delinsTG	ENSP00000493262.1:n.780+226_780+227delinsTG
ENST00000641721.1:n.644-632_644-631delinsTG
ENST00000641747.1:c.*292+226_*292+227delinsTG	ENSP00000493116.1:n.*292+226_*292+227delinsTG
ENST00000641759.1:n.915+226_915+227delinsTG
ENST00000641805.1:n.1063+226_1063+227delinsTG
ENST00000641820.1:c.45+226_45+227delinsTG	ENSP00000492937.1:n.45+226_45+227delinsTG
ENST00000376583.7:c.903+226_903+227delinsTG	ENSP00000365767.3:n.903+226_903+227delinsTG
ENST00000376585.5:c.903+226_903+227delinsTG	ENSP00000365770.1:n.903+226_903+227delinsTG
ENST00000376590.7:c.780+226_780+227delinsTG	ENSP00000365775.3:n.780+226_780+227delinsTG
ENST00000376592.5:c.780+226_780+227delinsTG	ENSP00000365777.1:n.780+226_780+227delinsTG
NM_005957.4:c.780+226_780+227delinsTG , LRG_726t1:c.780+226_780+227delinsTG	NP_005948.3:n.780+226_780+227delinsTG
XM_005263458.2:c.903+226_903+227delinsTG	XP_005263515.1:n.903+226_903+227delinsTG
XM_005263460.3:c.780+226_780+227delinsTG	XP_005263517.1:n.780+226_780+227delinsTG
XM_005263461.3:c.780+226_780+227delinsTG	XP_005263518.1:n.780+226_780+227delinsTG
XM_005263462.3:c.780+226_780+227delinsTG	XP_005263519.1:n.780+226_780+227delinsTG
XM_005263463.2:c.534+226_534+227delinsTG	XP_005263520.1:n.534+226_534+227delinsTG
XM_011541495.1:c.900+226_900+227delinsTG	XP_011539797.1:n.900+226_900+227delinsTG
XM_011541496.1:c.903+226_903+227delinsTG	XP_011539798.1:n.903+226_903+227delinsTG
NM_001330358.1:c.903+226_903+227delinsTG	NP_001317287.1:n.903+226_903+227delinsTG
XM_005263460.5:c.780+226_780+227delinsTG	XP_005263517.1:n.780+226_780+227delinsTG
XM_005263462.4:c.780+226_780+227delinsTG	XP_005263519.1:n.780+226_780+227delinsTG
XM_005263463.4:c.534+226_534+227delinsTG	XP_005263520.1:n.534+226_534+227delinsTG
XM_011541495.3:c.900+226_900+227delinsTG	XP_011539797.1:n.900+226_900+227delinsTG
XM_011541496.3:c.903+226_903+227delinsTG	XP_011539798.1:n.903+226_903+227delinsTG
XM_017001328.2:c.903+226_903+227delinsTG	XP_016856817.1:n.903+226_903+227delinsTG
XM_024447198.1:c.534+226_534+227delinsTG	XP_024302966.1:n.534+226_534+227delinsTG
XR_002956640.1:n.1647+226_1647+227delinsTG
NM_005957.5:c.780+226_780+227delinsTG MANE Select	NP_005948.3:n.780+226_780+227delinsTG
NM_001330358.2:c.903+226_903+227delinsTG	NP_001317287.1:n.903+226_903+227delinsTG