Canonical Allele Identifier: CA2574214286

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11794941_11794944dup , CM000663.2:g.11794941_11794944dup	GRCh38
NC_000001.10:g.11854998_11855001dup , CM000663.1:g.11854998_11855001dup	GRCh37
NC_000001.9:g.11777585_11777588dup	NCBI36
NG_013351.1:g.16160_16163dup , LRG_726:g.16160_16163dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.1155-81_1155-78dup	ENSP00000365770.1:n.1155-81_1155-78dup
ENST00000376590.9:c.1032-81_1032-78dup MANE Select	ENSP00000365775.3:n.1032-81_1032-78dup
ENST00000376592.6:c.1032-81_1032-78dup	ENSP00000365777.1:n.1032-81_1032-78dup
ENST00000423400.7:c.1152-81_1152-78dup	ENSP00000398908.3:n.1152-81_1152-78dup
ENST00000641407.1:c.1032-81_1032-78dup	ENSP00000493098.1:n.1032-81_1032-78dup
ENST00000641446.1:c.1032-81_1032-78dup	ENSP00000493262.1:n.1032-81_1032-78dup
ENST00000641747.1:c.*544-81_*544-78dup	ENSP00000493116.1:n.*544-81_*544-78dup
ENST00000641759.1:n.1320_1323dup
ENST00000641805.1:n.1468_1471dup
ENST00000641820.1:c.297-81_297-78dup	ENSP00000492937.1:n.297-81_297-78dup
ENST00000376583.7:c.1155-81_1155-78dup	ENSP00000365767.3:n.1155-81_1155-78dup
ENST00000376585.5:c.1155-81_1155-78dup	ENSP00000365770.1:n.1155-81_1155-78dup
ENST00000376590.7:c.1032-81_1032-78dup	ENSP00000365775.3:n.1032-81_1032-78dup
ENST00000376592.5:c.1032-81_1032-78dup	ENSP00000365777.1:n.1032-81_1032-78dup
NM_005957.4:c.1032-81_1032-78dup , LRG_726t1:c.1032-81_1032-78dup	NP_005948.3:n.1032-81_1032-78dup
XM_005263458.2:c.1155-81_1155-78dup	XP_005263515.1:n.1155-81_1155-78dup
XM_005263460.3:c.1032-81_1032-78dup	XP_005263517.1:n.1032-81_1032-78dup
XM_005263461.3:c.1032-81_1032-78dup	XP_005263518.1:n.1032-81_1032-78dup
XM_005263462.3:c.1032-81_1032-78dup	XP_005263519.1:n.1032-81_1032-78dup
XM_005263463.2:c.786-81_786-78dup	XP_005263520.1:n.786-81_786-78dup
XM_011541495.1:c.1152-81_1152-78dup	XP_011539797.1:n.1152-81_1152-78dup
XM_011541496.1:c.1155-81_1155-78dup	XP_011539798.1:n.1155-81_1155-78dup
NM_001330358.1:c.1155-81_1155-78dup	NP_001317287.1:n.1155-81_1155-78dup
XM_005263460.5:c.1032-81_1032-78dup	XP_005263517.1:n.1032-81_1032-78dup
XM_005263462.4:c.1032-81_1032-78dup	XP_005263519.1:n.1032-81_1032-78dup
XM_005263463.4:c.786-81_786-78dup	XP_005263520.1:n.786-81_786-78dup
XM_011541495.3:c.1152-81_1152-78dup	XP_011539797.1:n.1152-81_1152-78dup
XM_011541496.3:c.1155-81_1155-78dup	XP_011539798.1:n.1155-81_1155-78dup
XM_017001328.2:c.1155-81_1155-78dup	XP_016856817.1:n.1155-81_1155-78dup
XM_024447198.1:c.786-81_786-78dup	XP_024302966.1:n.786-81_786-78dup
XR_002956640.1:n.2052_2055dup
NM_005957.5:c.1032-81_1032-78dup MANE Select	NP_005948.3:n.1032-81_1032-78dup
NM_001330358.2:c.1155-81_1155-78dup	NP_001317287.1:n.1155-81_1155-78dup