Canonical Allele Identifier: CA338480296

Gene: MTHFR

Linked Data

• MyVariant Identifiers: chr1:g.11855300T>G (hg19) ; chr1:g.11795243T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11795243T>G , CM000663.2:g.11795243T>G	GRCh38
NC_000001.10:g.11855300T>G , CM000663.1:g.11855300T>G	GRCh37
NC_000001.9:g.11777887T>G	NCBI36
NG_013351.1:g.15861A>C , LRG_726:g.15861A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.1009A>C	ENSP00000365770.1:p.Asn337His
ENST00000376590.9:c.886A>C MANE Select	ENSP00000365775.3:p.Asn296His
ENST00000376592.6:c.886A>C	ENSP00000365777.1:p.Asn296His
ENST00000423400.7:c.1006A>C	ENSP00000398908.3:p.Asn336His
ENST00000641407.1:c.886A>C	ENSP00000493098.1:p.Asn296His
ENST00000641446.1:c.886A>C	ENSP00000493262.1:p.Asn296His
ENST00000641721.1:n.749A>C
ENST00000641747.1:c.*398A>C	ENSP00000493116.1:n.*398A>C
ENST00000641759.1:n.1021A>C
ENST00000641805.1:n.1169A>C
ENST00000641820.1:c.151A>C	ENSP00000492937.1:p.Asn51His
ENST00000376583.7:c.1009A>C	ENSP00000365767.3:p.Asn337His
ENST00000376585.5:c.1009A>C	ENSP00000365770.1:p.Asn337His
ENST00000376590.7:c.886A>C	ENSP00000365775.3:p.Asn296His
ENST00000376592.5:c.886A>C	ENSP00000365777.1:p.Asn296His
NM_005957.4:c.886A>C , LRG_726t1:c.886A>C	NP_005948.3:p.Asn296His
XM_005263458.2:c.1009A>C	XP_005263515.1:p.Asn337His
XM_005263460.3:c.886A>C	XP_005263517.1:p.Asn296His
XM_005263461.3:c.886A>C	XP_005263518.1:p.Asn296His
XM_005263462.3:c.886A>C	XP_005263519.1:p.Asn296His
XM_005263463.2:c.640A>C	XP_005263520.1:p.Asn214His
XM_011541495.1:c.1006A>C	XP_011539797.1:p.Asn336His
XM_011541496.1:c.1009A>C	XP_011539798.1:p.Asn337His
NM_001330358.1:c.1009A>C	NP_001317287.1:p.Asn337His
XM_005263460.5:c.886A>C	XP_005263517.1:p.Asn296His
XM_005263462.4:c.886A>C	XP_005263519.1:p.Asn296His
XM_005263463.4:c.640A>C	XP_005263520.1:p.Asn214His
XM_011541495.3:c.1006A>C	XP_011539797.1:p.Asn336His
XM_011541496.3:c.1009A>C	XP_011539798.1:p.Asn337His
XM_017001328.2:c.1009A>C	XP_016856817.1:p.Asn337His
XM_024447198.1:c.640A>C	XP_024302966.1:p.Asn214His
XR_002956640.1:n.1753A>C
NM_005957.5:c.886A>C MANE Select	NP_005948.3:p.Asn296His
NM_001330358.2:c.1009A>C	NP_001317287.1:p.Asn337His