Canonical Allele Identifier: CA416119546

Gene: MTHFR

Linked Data

• MyVariant Identifiers: chr1:g.11850803C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11790746C>G , CM000663.2:g.11790746C>G	GRCh38
NC_000001.10:g.11850803C>G , CM000663.1:g.11850803C>G	GRCh37
NC_000001.9:g.11773390C>G	NCBI36
NG_013351.1:g.20358G>C , LRG_726:g.20358G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376585.6:c.2028G>C	ENSP00000365770.1:p.Val676=
ENST00000376590.9:c.1905G>C MANE Select	ENSP00000365775.3:p.Val635=
ENST00000376592.6:c.1905G>C	ENSP00000365777.1:p.Val635=
ENST00000423400.7:c.2025G>C	ENSP00000398908.3:p.Val675=
ENST00000641407.1:c.1753-30G>C	ENSP00000493098.1:n.1753-30G>C
ENST00000641446.1:c.*364G>C	ENSP00000493262.1:n.*364G>C
ENST00000641747.1:c.*1417G>C	ENSP00000493116.1:n.*1417G>C
ENST00000641759.1:n.2274G>C
ENST00000641805.1:n.2270-30G>C
ENST00000641820.1:c.1170G>C	ENSP00000492937.1:p.Val390=
ENST00000376583.7:c.2028G>C	ENSP00000365767.3:p.Val676=
ENST00000376585.5:c.2028G>C	ENSP00000365770.1:p.Val676=
ENST00000376590.7:c.1905G>C	ENSP00000365775.3:p.Val635=
ENST00000376592.5:c.1905G>C	ENSP00000365777.1:p.Val635=
NM_005957.4:c.1905G>C , LRG_726t1:c.1905G>C	NP_005948.3:p.Val635=
XM_005263458.2:c.2028G>C	XP_005263515.1:p.Val676=
XM_005263460.3:c.1905G>C	XP_005263517.1:p.Val635=
XM_005263461.3:c.1905G>C	XP_005263518.1:p.Val635=
XM_005263462.3:c.1905G>C	XP_005263519.1:p.Val635=
XM_005263463.2:c.1659G>C	XP_005263520.1:p.Val553=
XM_011541495.1:c.2025G>C	XP_011539797.1:p.Val675=
XM_011541496.1:c.1876-30G>C	XP_011539798.1:n.1876-30G>C
NM_001330358.1:c.2028G>C	NP_001317287.1:p.Val676=
XM_005263460.5:c.1905G>C	XP_005263517.1:p.Val635=
XM_005263462.4:c.1905G>C	XP_005263519.1:p.Val635=
XM_005263463.4:c.1659G>C	XP_005263520.1:p.Val553=
XM_011541495.3:c.2025G>C	XP_011539797.1:p.Val675=
XM_011541496.3:c.1876-30G>C	XP_011539798.1:n.1876-30G>C
XM_017001328.2:c.1878G>C	XP_016856817.1:p.Val626=
XM_024447198.1:c.1659G>C	XP_024302966.1:p.Val553=
XR_002956640.1:n.2854-30G>C
NM_005957.5:c.1905G>C MANE Select	NP_005948.3:p.Val635=
NM_001330358.2:c.2028G>C	NP_001317287.1:p.Val676=