Canonical Allele Identifier: CA416362564

Gene: MTHFR

Linked Data

• ClinVar Variation Id: 1609888
• ClinVar RCV Id: RCV002152762
• dbSNP Id: rs2100527693
• MyVariant Identifiers: chr1:g.11854839T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11794782T>C , CM000663.2:g.11794782T>C	GRCh38
NC_000001.10:g.11854839T>C , CM000663.1:g.11854839T>C	GRCh37
NC_000001.9:g.11777426T>C	NCBI36
NG_013351.1:g.16322A>G , LRG_726:g.16322A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.1236A>G	ENSP00000365770.1:p.Pro412=
ENST00000376590.9:c.1113A>G MANE Select	ENSP00000365775.3:p.Pro371=
ENST00000376592.6:c.1113A>G	ENSP00000365777.1:p.Pro371=
ENST00000423400.7:c.1233A>G	ENSP00000398908.3:p.Pro411=
ENST00000641407.1:c.1113A>G	ENSP00000493098.1:p.Pro371=
ENST00000641446.1:c.1113A>G	ENSP00000493262.1:p.Pro371=
ENST00000641747.1:c.*625A>G	ENSP00000493116.1:n.*625A>G
ENST00000641759.1:n.1482A>G
ENST00000641805.1:n.1630A>G
ENST00000641820.1:c.378A>G	ENSP00000492937.1:p.Pro126=
ENST00000376583.7:c.1236A>G	ENSP00000365767.3:p.Pro412=
ENST00000376585.5:c.1236A>G	ENSP00000365770.1:p.Pro412=
ENST00000376590.7:c.1113A>G	ENSP00000365775.3:p.Pro371=
ENST00000376592.5:c.1113A>G	ENSP00000365777.1:p.Pro371=
NM_005957.4:c.1113A>G , LRG_726t1:c.1113A>G	NP_005948.3:p.Pro371=
XM_005263458.2:c.1236A>G	XP_005263515.1:p.Pro412=
XM_005263460.3:c.1113A>G	XP_005263517.1:p.Pro371=
XM_005263461.3:c.1113A>G	XP_005263518.1:p.Pro371=
XM_005263462.3:c.1113A>G	XP_005263519.1:p.Pro371=
XM_005263463.2:c.867A>G	XP_005263520.1:p.Pro289=
XM_011541495.1:c.1233A>G	XP_011539797.1:p.Pro411=
XM_011541496.1:c.1236A>G	XP_011539798.1:p.Pro412=
NM_001330358.1:c.1236A>G	NP_001317287.1:p.Pro412=
XM_005263460.5:c.1113A>G	XP_005263517.1:p.Pro371=
XM_005263462.4:c.1113A>G	XP_005263519.1:p.Pro371=
XM_005263463.4:c.867A>G	XP_005263520.1:p.Pro289=
XM_011541495.3:c.1233A>G	XP_011539797.1:p.Pro411=
XM_011541496.3:c.1236A>G	XP_011539798.1:p.Pro412=
XM_017001328.2:c.1236A>G	XP_016856817.1:p.Pro412=
XM_024447198.1:c.867A>G	XP_024302966.1:p.Pro289=
XR_002956640.1:n.2214A>G
NM_005957.5:c.1113A>G MANE Select	NP_005948.3:p.Pro371=
NM_001330358.2:c.1236A>G	NP_001317287.1:p.Pro412=