Canonical Allele Identifier: CA338422225

Gene: MTHFR

Linked Data

• gnomAD v4: 1-11801199-T-C
• COSMIC: COSM4140768 ; COSM4140769
• MyVariant Identifiers: chr1:g.11861256T>C (hg19) ; chr1:g.11801199T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11801199T>C , CM000663.2:g.11801199T>C	GRCh38
NC_000001.10:g.11861256T>C , CM000663.1:g.11861256T>C	GRCh37
NC_000001.9:g.11783843T>C	NCBI36
NG_008766.1:g.50T>C
NG_013351.1:g.9905A>G , LRG_726:g.9905A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376486.3:c.437A>G	ENSP00000365669.3:p.Lys146Arg
ENST00000376585.6:c.560A>G	ENSP00000365770.1:p.Lys187Arg
ENST00000376590.9:c.437A>G MANE Select	ENSP00000365775.3:p.Lys146Arg
ENST00000376592.6:c.437A>G	ENSP00000365777.1:p.Lys146Arg
ENST00000423400.7:c.557A>G	ENSP00000398908.3:p.Lys186Arg
ENST00000641407.1:c.437A>G	ENSP00000493098.1:p.Lys146Arg
ENST00000641437.1:n.569A>G
ENST00000641446.1:c.437A>G	ENSP00000493262.1:p.Lys146Arg
ENST00000641721.1:n.494A>G
ENST00000641747.1:c.237-877A>G	ENSP00000493116.1:n.237-877A>G
ENST00000641759.1:n.572A>G
ENST00000641805.1:n.720A>G
ENST00000641909.1:n.847A>G
ENST00000376583.7:c.560A>G	ENSP00000365767.3:p.Lys187Arg
ENST00000376585.5:c.560A>G	ENSP00000365770.1:p.Lys187Arg
ENST00000376590.7:c.437A>G	ENSP00000365775.3:p.Lys146Arg
ENST00000376592.5:c.437A>G	ENSP00000365777.1:p.Lys146Arg
NM_005957.4:c.437A>G , LRG_726t1:c.437A>G	NP_005948.3:p.Lys146Arg
XM_005263458.2:c.560A>G	XP_005263515.1:p.Lys187Arg
XM_005263460.3:c.437A>G	XP_005263517.1:p.Lys146Arg
XM_005263461.3:c.437A>G	XP_005263518.1:p.Lys146Arg
XM_005263462.3:c.437A>G	XP_005263519.1:p.Lys146Arg
XM_005263463.2:c.191A>G	XP_005263520.1:p.Lys64Arg
XM_011541495.1:c.557A>G	XP_011539797.1:p.Lys186Arg
XM_011541496.1:c.560A>G	XP_011539798.1:p.Lys187Arg
NM_001330358.1:c.560A>G	NP_001317287.1:p.Lys187Arg
XM_005263460.5:c.437A>G	XP_005263517.1:p.Lys146Arg
XM_005263462.4:c.437A>G	XP_005263519.1:p.Lys146Arg
XM_005263463.4:c.191A>G	XP_005263520.1:p.Lys64Arg
XM_011541495.3:c.557A>G	XP_011539797.1:p.Lys186Arg
XM_011541496.3:c.560A>G	XP_011539798.1:p.Lys187Arg
XM_017001328.2:c.560A>G	XP_016856817.1:p.Lys187Arg
XM_024447198.1:c.191A>G	XP_024302966.1:p.Lys64Arg
XR_002956640.1:n.1304A>G
NM_005957.5:c.437A>G MANE Select	NP_005948.3:p.Lys146Arg
NM_001330358.2:c.560A>G	NP_001317287.1:p.Lys187Arg