Canonical Allele Identifier: CA338480924

Gene: MTHFR

Linked Data

• MyVariant Identifiers: chr1:g.11856402A>C (hg19) ; chr1:g.11796345A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11796345A>C , CM000663.2:g.11796345A>C	GRCh38
NC_000001.10:g.11856402A>C , CM000663.1:g.11856402A>C	GRCh37
NC_000001.9:g.11778989A>C	NCBI36
NG_013351.1:g.14759T>G , LRG_726:g.14759T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376486.3:c.641T>G	ENSP00000365669.3:p.Leu214Trp
ENST00000376585.6:c.764T>G	ENSP00000365770.1:p.Leu255Trp
ENST00000376590.9:c.641T>G MANE Select	ENSP00000365775.3:p.Leu214Trp
ENST00000376592.6:c.641T>G	ENSP00000365777.1:p.Leu214Trp
ENST00000423400.7:c.761T>G	ENSP00000398908.3:p.Leu254Trp
ENST00000641407.1:c.641T>G	ENSP00000493098.1:p.Leu214Trp
ENST00000641446.1:c.641T>G	ENSP00000493262.1:p.Leu214Trp
ENST00000641721.1:n.644-997T>G
ENST00000641747.1:c.*153T>G	ENSP00000493116.1:n.*153T>G
ENST00000641759.1:n.776T>G
ENST00000641805.1:n.924T>G
ENST00000641820.1:c.-95T>G	ENSP00000492937.1:n.-95T>G
ENST00000376583.7:c.764T>G	ENSP00000365767.3:p.Leu255Trp
ENST00000376585.5:c.764T>G	ENSP00000365770.1:p.Leu255Trp
ENST00000376590.7:c.641T>G	ENSP00000365775.3:p.Leu214Trp
ENST00000376592.5:c.641T>G	ENSP00000365777.1:p.Leu214Trp
NM_005957.4:c.641T>G , LRG_726t1:c.641T>G	NP_005948.3:p.Leu214Trp
XM_005263458.2:c.764T>G	XP_005263515.1:p.Leu255Trp
XM_005263460.3:c.641T>G	XP_005263517.1:p.Leu214Trp
XM_005263461.3:c.641T>G	XP_005263518.1:p.Leu214Trp
XM_005263462.3:c.641T>G	XP_005263519.1:p.Leu214Trp
XM_005263463.2:c.395T>G	XP_005263520.1:p.Leu132Trp
XM_011541495.1:c.761T>G	XP_011539797.1:p.Leu254Trp
XM_011541496.1:c.764T>G	XP_011539798.1:p.Leu255Trp
NM_001330358.1:c.764T>G	NP_001317287.1:p.Leu255Trp
XM_005263460.5:c.641T>G	XP_005263517.1:p.Leu214Trp
XM_005263462.4:c.641T>G	XP_005263519.1:p.Leu214Trp
XM_005263463.4:c.395T>G	XP_005263520.1:p.Leu132Trp
XM_011541495.3:c.761T>G	XP_011539797.1:p.Leu254Trp
XM_011541496.3:c.764T>G	XP_011539798.1:p.Leu255Trp
XM_017001328.2:c.764T>G	XP_016856817.1:p.Leu255Trp
XM_024447198.1:c.395T>G	XP_024302966.1:p.Leu132Trp
XR_002956640.1:n.1508T>G
NM_005957.5:c.641T>G MANE Select	NP_005948.3:p.Leu214Trp
NM_001330358.2:c.764T>G	NP_001317287.1:p.Leu255Trp