Canonical Allele Identifier: CA1153794922

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11792540_11792542delinsTTC , CM000663.2:g.11792540_11792542delinsTTC	GRCh38
NC_000001.10:g.11852597_11852599delinsTTC , CM000663.1:g.11852597_11852599delinsTTC	GRCh37
NC_000001.9:g.11775184_11775186delinsTTC	NCBI36
NG_013351.1:g.18562_18564delinsGAA , LRG_726:g.18562_18564delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.1654-163_1654-161delinsGAA	ENSP00000365770.1:n.1654-163_1654-161delinsGAA
ENST00000376590.9:c.1531-163_1531-161delinsGAA MANE Select	ENSP00000365775.3:n.1531-163_1531-161delinsGAA
ENST00000376592.6:c.1531-163_1531-161delinsGAA	ENSP00000365777.1:n.1531-163_1531-161delinsGAA
ENST00000423400.7:c.1651-163_1651-161delinsGAA	ENSP00000398908.3:n.1651-163_1651-161delinsGAA
ENST00000641407.1:c.1531-163_1531-161delinsGAA	ENSP00000493098.1:n.1531-163_1531-161delinsGAA
ENST00000641446.1:c.1531-163_1531-161delinsGAA	ENSP00000493262.1:n.1531-163_1531-161delinsGAA
ENST00000641747.1:c.*1043-163_*1043-161delinsGAA	ENSP00000493116.1:n.*1043-163_*1043-161delinsGAA
ENST00000641759.1:n.1900-163_1900-161delinsGAA
ENST00000641805.1:n.2048-163_2048-161delinsGAA
ENST00000641820.1:c.796-163_796-161delinsGAA	ENSP00000492937.1:n.796-163_796-161delinsGAA
ENST00000376583.7:c.1654-163_1654-161delinsGAA	ENSP00000365767.3:n.1654-163_1654-161delinsGAA
ENST00000376585.5:c.1654-163_1654-161delinsGAA	ENSP00000365770.1:n.1654-163_1654-161delinsGAA
ENST00000376590.7:c.1531-163_1531-161delinsGAA	ENSP00000365775.3:n.1531-163_1531-161delinsGAA
ENST00000376592.5:c.1531-163_1531-161delinsGAA	ENSP00000365777.1:n.1531-163_1531-161delinsGAA
NM_005957.4:c.1531-163_1531-161delinsGAA , LRG_726t1:c.1531-163_1531-161delinsGAA	NP_005948.3:n.1531-163_1531-161delinsGAA
XM_005263458.2:c.1654-163_1654-161delinsGAA	XP_005263515.1:n.1654-163_1654-161delinsGAA
XM_005263460.3:c.1531-163_1531-161delinsGAA	XP_005263517.1:n.1531-163_1531-161delinsGAA
XM_005263461.3:c.1531-163_1531-161delinsGAA	XP_005263518.1:n.1531-163_1531-161delinsGAA
XM_005263462.3:c.1531-163_1531-161delinsGAA	XP_005263519.1:n.1531-163_1531-161delinsGAA
XM_005263463.2:c.1285-163_1285-161delinsGAA	XP_005263520.1:n.1285-163_1285-161delinsGAA
XM_011541495.1:c.1651-163_1651-161delinsGAA	XP_011539797.1:n.1651-163_1651-161delinsGAA
XM_011541496.1:c.1654-163_1654-161delinsGAA	XP_011539798.1:n.1654-163_1654-161delinsGAA
NM_001330358.1:c.1654-163_1654-161delinsGAA	NP_001317287.1:n.1654-163_1654-161delinsGAA
XM_005263460.5:c.1531-163_1531-161delinsGAA	XP_005263517.1:n.1531-163_1531-161delinsGAA
XM_005263462.4:c.1531-163_1531-161delinsGAA	XP_005263519.1:n.1531-163_1531-161delinsGAA
XM_005263463.4:c.1285-163_1285-161delinsGAA	XP_005263520.1:n.1285-163_1285-161delinsGAA
XM_011541495.3:c.1651-163_1651-161delinsGAA	XP_011539797.1:n.1651-163_1651-161delinsGAA
XM_011541496.3:c.1654-163_1654-161delinsGAA	XP_011539798.1:n.1654-163_1654-161delinsGAA
XM_017001328.2:c.1654-163_1654-161delinsGAA	XP_016856817.1:n.1654-163_1654-161delinsGAA
XM_024447198.1:c.1285-163_1285-161delinsGAA	XP_024302966.1:n.1285-163_1285-161delinsGAA
XR_002956640.1:n.2632-163_2632-161delinsGAA
NM_005957.5:c.1531-163_1531-161delinsGAA MANE Select	NP_005948.3:n.1531-163_1531-161delinsGAA
NM_001330358.2:c.1654-163_1654-161delinsGAA	NP_001317287.1:n.1654-163_1654-161delinsGAA