Canonical Allele Identifier: CA338422191

Gene: MTHFR

Linked Data

• MyVariant Identifiers: chr1:g.11861239T>C (hg19) ; chr1:g.11801182T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11801182T>C , CM000663.2:g.11801182T>C	GRCh38
NC_000001.10:g.11861239T>C , CM000663.1:g.11861239T>C	GRCh37
NC_000001.9:g.11783826T>C	NCBI36
NG_008766.1:g.33T>C
NG_013351.1:g.9922A>G , LRG_726:g.9922A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376486.3:c.454A>G	ENSP00000365669.3:p.Asn152Asp
ENST00000376585.6:c.577A>G	ENSP00000365770.1:p.Asn193Asp
ENST00000376590.9:c.454A>G MANE Select	ENSP00000365775.3:p.Asn152Asp
ENST00000376592.6:c.454A>G	ENSP00000365777.1:p.Asn152Asp
ENST00000423400.7:c.574A>G	ENSP00000398908.3:p.Asn192Asp
ENST00000641407.1:c.454A>G	ENSP00000493098.1:p.Asn152Asp
ENST00000641437.1:n.586A>G
ENST00000641446.1:c.454A>G	ENSP00000493262.1:p.Asn152Asp
ENST00000641721.1:n.511A>G
ENST00000641747.1:c.237-860A>G	ENSP00000493116.1:n.237-860A>G
ENST00000641759.1:n.589A>G
ENST00000641805.1:n.737A>G
ENST00000641909.1:n.864A>G
ENST00000376583.7:c.577A>G	ENSP00000365767.3:p.Asn193Asp
ENST00000376585.5:c.577A>G	ENSP00000365770.1:p.Asn193Asp
ENST00000376590.7:c.454A>G	ENSP00000365775.3:p.Asn152Asp
ENST00000376592.5:c.454A>G	ENSP00000365777.1:p.Asn152Asp
NM_005957.4:c.454A>G , LRG_726t1:c.454A>G	NP_005948.3:p.Asn152Asp
XM_005263458.2:c.577A>G	XP_005263515.1:p.Asn193Asp
XM_005263460.3:c.454A>G	XP_005263517.1:p.Asn152Asp
XM_005263461.3:c.454A>G	XP_005263518.1:p.Asn152Asp
XM_005263462.3:c.454A>G	XP_005263519.1:p.Asn152Asp
XM_005263463.2:c.208A>G	XP_005263520.1:p.Asn70Asp
XM_011541495.1:c.574A>G	XP_011539797.1:p.Asn192Asp
XM_011541496.1:c.577A>G	XP_011539798.1:p.Asn193Asp
NM_001330358.1:c.577A>G	NP_001317287.1:p.Asn193Asp
XM_005263460.5:c.454A>G	XP_005263517.1:p.Asn152Asp
XM_005263462.4:c.454A>G	XP_005263519.1:p.Asn152Asp
XM_005263463.4:c.208A>G	XP_005263520.1:p.Asn70Asp
XM_011541495.3:c.574A>G	XP_011539797.1:p.Asn192Asp
XM_011541496.3:c.577A>G	XP_011539798.1:p.Asn193Asp
XM_017001328.2:c.577A>G	XP_016856817.1:p.Asn193Asp
XM_024447198.1:c.208A>G	XP_024302966.1:p.Asn70Asp
XR_002956640.1:n.1321A>G
NM_005957.5:c.454A>G MANE Select	NP_005948.3:p.Asn152Asp
NM_001330358.2:c.577A>G	NP_001317287.1:p.Asn193Asp