Canonical Allele Identifier: CA338474341

Gene: MTHFR

Linked Data

• MyVariant Identifiers: chr1:g.11851287G>A (hg19) ; chr1:g.11791230G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11791230G>A , CM000663.2:g.11791230G>A	GRCh38
NC_000001.10:g.11851287G>A , CM000663.1:g.11851287G>A	GRCh37
NC_000001.9:g.11773874G>A	NCBI36
NG_013351.1:g.19874C>T , LRG_726:g.19874C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.1852C>T	ENSP00000365770.1:p.Pro618Ser
ENST00000376590.9:c.1729C>T MANE Select	ENSP00000365775.3:p.Pro577Ser
ENST00000376592.6:c.1729C>T	ENSP00000365777.1:p.Pro577Ser
ENST00000423400.7:c.1849C>T	ENSP00000398908.3:p.Pro617Ser
ENST00000641407.1:c.1729C>T	ENSP00000493098.1:p.Pro577Ser
ENST00000641446.1:c.*188C>T	ENSP00000493262.1:n.*188C>T
ENST00000641747.1:c.*1241C>T	ENSP00000493116.1:n.*1241C>T
ENST00000641759.1:n.2098C>T
ENST00000641805.1:n.2246C>T
ENST00000641820.1:c.994C>T	ENSP00000492937.1:p.Pro332Ser
ENST00000376583.7:c.1852C>T	ENSP00000365767.3:p.Pro618Ser
ENST00000376585.5:c.1852C>T	ENSP00000365770.1:p.Pro618Ser
ENST00000376590.7:c.1729C>T	ENSP00000365775.3:p.Pro577Ser
ENST00000376592.5:c.1729C>T	ENSP00000365777.1:p.Pro577Ser
NM_005957.4:c.1729C>T , LRG_726t1:c.1729C>T	NP_005948.3:p.Pro577Ser
XM_005263458.2:c.1852C>T	XP_005263515.1:p.Pro618Ser
XM_005263460.3:c.1729C>T	XP_005263517.1:p.Pro577Ser
XM_005263461.3:c.1729C>T	XP_005263518.1:p.Pro577Ser
XM_005263462.3:c.1729C>T	XP_005263519.1:p.Pro577Ser
XM_005263463.2:c.1483C>T	XP_005263520.1:p.Pro495Ser
XM_011541495.1:c.1849C>T	XP_011539797.1:p.Pro617Ser
XM_011541496.1:c.1852C>T	XP_011539798.1:p.Pro618Ser
NM_001330358.1:c.1852C>T	NP_001317287.1:p.Pro618Ser
XM_005263460.5:c.1729C>T	XP_005263517.1:p.Pro577Ser
XM_005263462.4:c.1729C>T	XP_005263519.1:p.Pro577Ser
XM_005263463.4:c.1483C>T	XP_005263520.1:p.Pro495Ser
XM_011541495.3:c.1849C>T	XP_011539797.1:p.Pro617Ser
XM_011541496.3:c.1852C>T	XP_011539798.1:p.Pro618Ser
XM_017001328.2:c.1852C>T	XP_016856817.1:p.Pro618Ser
XM_024447198.1:c.1483C>T	XP_024302966.1:p.Pro495Ser
XR_002956640.1:n.2830C>T
NM_005957.5:c.1729C>T MANE Select	NP_005948.3:p.Pro577Ser
NM_001330358.2:c.1852C>T	NP_001317287.1:p.Pro618Ser