Canonical Allele Identifier: CA416360675

Gene: MTHFR

Linked Data

• MyVariant Identifiers: chr1:g.11863158T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11803101T>G , CM000663.2:g.11803101T>G	GRCh38
NC_000001.10:g.11863158T>G , CM000663.1:g.11863158T>G	GRCh37
NC_000001.9:g.11785745T>G	NCBI36
NG_008766.1:g.1952T>G
NG_013351.1:g.8003A>C , LRG_726:g.8003A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376486.3:c.16A>C	ENSP00000365669.3:p.Arg6=
ENST00000376585.6:c.139A>C	ENSP00000365770.1:p.Arg47=
ENST00000376590.9:c.16A>C MANE Select	ENSP00000365775.3:p.Arg6=
ENST00000376592.6:c.16A>C	ENSP00000365777.1:p.Arg6=
ENST00000423400.7:c.136A>C	ENSP00000398908.3:p.Arg46=
ENST00000431243.6:n.797A>C
ENST00000641407.1:c.16A>C	ENSP00000493098.1:p.Arg6=
ENST00000641437.1:n.148A>C
ENST00000641446.1:c.16A>C	ENSP00000493262.1:p.Arg6=
ENST00000641721.1:n.73A>C
ENST00000641747.1:c.16A>C	ENSP00000493116.1:p.Arg6=
ENST00000641759.1:n.151A>C
ENST00000641805.1:n.299A>C
ENST00000641909.1:n.426A>C
ENST00000642002.1:n.245A>C
ENST00000376486.2:c.16A>C	ENSP00000365669.2:p.Arg6=
ENST00000376583.7:c.139A>C	ENSP00000365767.3:p.Arg47=
ENST00000376585.5:c.139A>C	ENSP00000365770.1:p.Arg47=
ENST00000376590.7:c.16A>C	ENSP00000365775.3:p.Arg6=
ENST00000376592.5:c.16A>C	ENSP00000365777.1:p.Arg6=
ENST00000413656.5:c.16A>C	ENSP00000408307.1:p.Arg6=
ENST00000418034.1:c.16A>C	ENSP00000405082.1:p.Arg6=
ENST00000423400.5:c.85A>C	ENSP00000398908.1:p.Arg29=
ENST00000431243.5:c.16A>C	ENSP00000400460.1:p.Arg6=
NM_005957.4:c.16A>C , LRG_726t1:c.16A>C	NP_005948.3:p.Arg6=
XM_005263458.2:c.139A>C	XP_005263515.1:p.Arg47=
XM_005263460.3:c.16A>C	XP_005263517.1:p.Arg6=
XM_005263461.3:c.16A>C	XP_005263518.1:p.Arg6=
XM_005263462.3:c.16A>C	XP_005263519.1:p.Arg6=
XM_005263463.2:c.-248A>C	XP_005263520.1:n.-248A>C
XM_011541495.1:c.136A>C	XP_011539797.1:p.Arg46=
XM_011541496.1:c.139A>C	XP_011539798.1:p.Arg47=
NM_001330358.1:c.139A>C	NP_001317287.1:p.Arg47=
XM_005263460.5:c.16A>C	XP_005263517.1:p.Arg6=
XM_005263462.4:c.16A>C	XP_005263519.1:p.Arg6=
XM_005263463.4:c.-248A>C	XP_005263520.1:n.-248A>C
XM_011541495.3:c.136A>C	XP_011539797.1:p.Arg46=
XM_011541496.3:c.139A>C	XP_011539798.1:p.Arg47=
XM_017001328.2:c.139A>C	XP_016856817.1:p.Arg47=
XM_024447198.1:c.-248A>C	XP_024302966.1:n.-248A>C
XR_002956640.1:n.883A>C
NM_005957.5:c.16A>C MANE Select	NP_005948.3:p.Arg6=
NM_001330358.2:c.139A>C	NP_001317287.1:p.Arg47=