Canonical Allele Identifier: CA338422017

Gene: MTHFR

Linked Data

• MyVariant Identifiers: chr1:g.11860328A>G (hg19) ; chr1:g.11800271A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11800271A>G , CM000663.2:g.11800271A>G	GRCh38
NC_000001.10:g.11860328A>G , CM000663.1:g.11860328A>G	GRCh37
NC_000001.9:g.11782915A>G	NCBI36
NG_013351.1:g.10833T>C , LRG_726:g.10833T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376486.3:c.527T>C	ENSP00000365669.3:p.Val176Ala
ENST00000376585.6:c.650T>C	ENSP00000365770.1:p.Val217Ala
ENST00000376590.9:c.527T>C MANE Select	ENSP00000365775.3:p.Val176Ala
ENST00000376592.6:c.527T>C	ENSP00000365777.1:p.Val176Ala
ENST00000423400.7:c.647T>C	ENSP00000398908.3:p.Val216Ala
ENST00000641407.1:c.527T>C	ENSP00000493098.1:p.Val176Ala
ENST00000641437.1:n.1497T>C
ENST00000641446.1:c.527T>C	ENSP00000493262.1:p.Val176Ala
ENST00000641721.1:n.584T>C
ENST00000641747.1:c.*39T>C	ENSP00000493116.1:n.*39T>C
ENST00000641759.1:n.662T>C
ENST00000641805.1:n.810T>C
ENST00000641909.1:n.1775T>C
ENST00000376583.7:c.650T>C	ENSP00000365767.3:p.Val217Ala
ENST00000376585.5:c.650T>C	ENSP00000365770.1:p.Val217Ala
ENST00000376590.7:c.527T>C	ENSP00000365775.3:p.Val176Ala
ENST00000376592.5:c.527T>C	ENSP00000365777.1:p.Val176Ala
NM_005957.4:c.527T>C , LRG_726t1:c.527T>C	NP_005948.3:p.Val176Ala
XM_005263458.2:c.650T>C	XP_005263515.1:p.Val217Ala
XM_005263460.3:c.527T>C	XP_005263517.1:p.Val176Ala
XM_005263461.3:c.527T>C	XP_005263518.1:p.Val176Ala
XM_005263462.3:c.527T>C	XP_005263519.1:p.Val176Ala
XM_005263463.2:c.281T>C	XP_005263520.1:p.Val94Ala
XM_011541495.1:c.647T>C	XP_011539797.1:p.Val216Ala
XM_011541496.1:c.650T>C	XP_011539798.1:p.Val217Ala
NM_001330358.1:c.650T>C	NP_001317287.1:p.Val217Ala
XM_005263460.5:c.527T>C	XP_005263517.1:p.Val176Ala
XM_005263462.4:c.527T>C	XP_005263519.1:p.Val176Ala
XM_005263463.4:c.281T>C	XP_005263520.1:p.Val94Ala
XM_011541495.3:c.647T>C	XP_011539797.1:p.Val216Ala
XM_011541496.3:c.650T>C	XP_011539798.1:p.Val217Ala
XM_017001328.2:c.650T>C	XP_016856817.1:p.Val217Ala
XM_024447198.1:c.281T>C	XP_024302966.1:p.Val94Ala
XR_002956640.1:n.1394T>C
NM_005957.5:c.527T>C MANE Select	NP_005948.3:p.Val176Ala
NM_001330358.2:c.650T>C	NP_001317287.1:p.Val217Ala