Canonical Allele Identifier: CA2643297084

Gene: MTHFR

Linked Data

• gnomAD v4: 1-11796569-T-TATGA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11796569_11796570insATGA , CM000663.2:g.11796569_11796570insATGA	GRCh38
NC_000001.10:g.11856626_11856627insATGA , CM000663.1:g.11856626_11856627insATGA	GRCh37
NC_000001.9:g.11779213_11779214insATGA	NCBI36
NG_013351.1:g.14534_14535insTCAT , LRG_726:g.14534_14535insTCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376486.3:c.587-171_587-170insTCAT	ENSP00000365669.3:n.587-171_587-170insTCAT
ENST00000376585.6:c.710-171_710-170insTCAT	ENSP00000365770.1:n.710-171_710-170insTCAT
ENST00000376590.9:c.587-171_587-170insTCAT MANE Select	ENSP00000365775.3:n.587-171_587-170insTCAT
ENST00000376592.6:c.587-171_587-170insTCAT	ENSP00000365777.1:n.587-171_587-170insTCAT
ENST00000423400.7:c.707-171_707-170insTCAT	ENSP00000398908.3:n.707-171_707-170insTCAT
ENST00000641407.1:c.587-171_587-170insTCAT	ENSP00000493098.1:n.587-171_587-170insTCAT
ENST00000641446.1:c.587-171_587-170insTCAT	ENSP00000493262.1:n.587-171_587-170insTCAT
ENST00000641721.1:n.644-1222_644-1221insTCAT
ENST00000641747.1:c.*99-171_*99-170insTCAT	ENSP00000493116.1:n.*99-171_*99-170insTCAT
ENST00000641759.1:n.722-171_722-170insTCAT
ENST00000641805.1:n.870-171_870-170insTCAT
ENST00000376583.7:c.710-171_710-170insTCAT	ENSP00000365767.3:n.710-171_710-170insTCAT
ENST00000376585.5:c.710-171_710-170insTCAT	ENSP00000365770.1:n.710-171_710-170insTCAT
ENST00000376590.7:c.587-171_587-170insTCAT	ENSP00000365775.3:n.587-171_587-170insTCAT
ENST00000376592.5:c.587-171_587-170insTCAT	ENSP00000365777.1:n.587-171_587-170insTCAT
NM_005957.4:c.587-171_587-170insTCAT , LRG_726t1:c.587-171_587-170insTCAT	NP_005948.3:n.587-171_587-170insTCAT
XM_005263458.2:c.710-171_710-170insTCAT	XP_005263515.1:n.710-171_710-170insTCAT
XM_005263460.3:c.587-171_587-170insTCAT	XP_005263517.1:n.587-171_587-170insTCAT
XM_005263461.3:c.587-171_587-170insTCAT	XP_005263518.1:n.587-171_587-170insTCAT
XM_005263462.3:c.587-171_587-170insTCAT	XP_005263519.1:n.587-171_587-170insTCAT
XM_005263463.2:c.341-171_341-170insTCAT	XP_005263520.1:n.341-171_341-170insTCAT
XM_011541495.1:c.707-171_707-170insTCAT	XP_011539797.1:n.707-171_707-170insTCAT
XM_011541496.1:c.710-171_710-170insTCAT	XP_011539798.1:n.710-171_710-170insTCAT
NM_001330358.1:c.710-171_710-170insTCAT	NP_001317287.1:n.710-171_710-170insTCAT
XM_005263460.5:c.587-171_587-170insTCAT	XP_005263517.1:n.587-171_587-170insTCAT
XM_005263462.4:c.587-171_587-170insTCAT	XP_005263519.1:n.587-171_587-170insTCAT
XM_005263463.4:c.341-171_341-170insTCAT	XP_005263520.1:n.341-171_341-170insTCAT
XM_011541495.3:c.707-171_707-170insTCAT	XP_011539797.1:n.707-171_707-170insTCAT
XM_011541496.3:c.710-171_710-170insTCAT	XP_011539798.1:n.710-171_710-170insTCAT
XM_017001328.2:c.710-171_710-170insTCAT	XP_016856817.1:n.710-171_710-170insTCAT
XM_024447198.1:c.341-171_341-170insTCAT	XP_024302966.1:n.341-171_341-170insTCAT
XR_002956640.1:n.1454-171_1454-170insTCAT
NM_005957.5:c.587-171_587-170insTCAT MANE Select	NP_005948.3:n.587-171_587-170insTCAT
NM_001330358.2:c.710-171_710-170insTCAT	NP_001317287.1:n.710-171_710-170insTCAT