Canonical Allele Identifier: CA1153790106

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11790395_11790398delinsCAGG , CM000663.2:g.11790395_11790398delinsCAGG	GRCh38
NC_000001.10:g.11850452_11850455delinsCAGG , CM000663.1:g.11850452_11850455delinsCAGG	GRCh37
NC_000001.9:g.11773039_11773042delinsCAGG	NCBI36
NG_013351.1:g.20706_20709delinsCCTG , LRG_726:g.20706_20709delinsCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.*282_*285delinsCCTG	ENSP00000365770.1:n.*282_*285delinsCCTG
ENST00000376590.9:c.*282_*285delinsCCTG MANE Select	ENSP00000365775.3:n.*282_*285delinsCCTG
ENST00000376592.6:c.*282_*285delinsCCTG	ENSP00000365777.1:n.*282_*285delinsCCTG
ENST00000423400.7:c.*282_*285delinsCCTG	ENSP00000398908.3:n.*282_*285delinsCCTG
ENST00000641407.1:c.*142_*145delinsCCTG	ENSP00000493098.1:n.*142_*145delinsCCTG
ENST00000641446.1:c.*712_*715delinsCCTG	ENSP00000493262.1:n.*712_*715delinsCCTG
ENST00000641747.1:c.*1765_*1768delinsCCTG	ENSP00000493116.1:n.*1765_*1768delinsCCTG
ENST00000641805.1:n.2588_2591delinsCCTG
ENST00000376583.7:c.2376_2379delinsCCTG	ENSP00000365767.3:n.2376_2379delinsCCTG
ENST00000376585.5:c.*282_*285delinsCCTG	ENSP00000365770.1:n.*282_*285delinsCCTG
ENST00000376590.7:c.*282_*285delinsCCTG	ENSP00000365775.3:n.*282_*285delinsCCTG
ENST00000376592.5:c.*282_*285delinsCCTG	ENSP00000365777.1:n.*282_*285delinsCCTG
NM_005957.4:c.*282_*285delinsCCTG , LRG_726t1:c.*282_*285delinsCCTG	NP_005948.3:n.*282_*285delinsCCTG
XM_005263458.2:c.*282_*285delinsCCTG	XP_005263515.1:n.*282_*285delinsCCTG
XM_005263460.3:c.*282_*285delinsCCTG	XP_005263517.1:n.*282_*285delinsCCTG
XM_005263461.3:c.*282_*285delinsCCTG	XP_005263518.1:n.*282_*285delinsCCTG
XM_005263462.3:c.*282_*285delinsCCTG	XP_005263519.1:n.*282_*285delinsCCTG
XM_005263463.2:c.*282_*285delinsCCTG	XP_005263520.1:n.*282_*285delinsCCTG
XM_011541495.1:c.*282_*285delinsCCTG	XP_011539797.1:n.*282_*285delinsCCTG
XM_011541496.1:c.*142_*145delinsCCTG	XP_011539798.1:n.*142_*145delinsCCTG
NM_001330358.1:c.*282_*285delinsCCTG	NP_001317287.1:n.*282_*285delinsCCTG
XM_005263460.5:c.*282_*285delinsCCTG	XP_005263517.1:n.*282_*285delinsCCTG
XM_005263462.4:c.*282_*285delinsCCTG	XP_005263519.1:n.*282_*285delinsCCTG
XM_005263463.4:c.*282_*285delinsCCTG	XP_005263520.1:n.*282_*285delinsCCTG
XM_011541495.3:c.*282_*285delinsCCTG	XP_011539797.1:n.*282_*285delinsCCTG
XM_011541496.3:c.*142_*145delinsCCTG	XP_011539798.1:n.*142_*145delinsCCTG
XM_024447198.1:c.*282_*285delinsCCTG	XP_024302966.1:n.*282_*285delinsCCTG
NM_005957.5:c.*282_*285delinsCCTG MANE Select	NP_005948.3:n.*282_*285delinsCCTG
NM_001330358.2:c.*282_*285delinsCCTG	NP_001317287.1:n.*282_*285delinsCCTG