Canonical Allele Identifier: CA338480584

Gene: MTHFR

Linked Data

• ClinVar Variation Id: 2627418
• ClinVar RCV Id: RCV003388681
• MyVariant Identifiers: chr1:g.11856288A>C (hg19) ; chr1:g.11796231A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11796231A>C , CM000663.2:g.11796231A>C	GRCh38
NC_000001.10:g.11856288A>C , CM000663.1:g.11856288A>C	GRCh37
NC_000001.9:g.11778875A>C	NCBI36
NG_013351.1:g.14873T>G , LRG_726:g.14873T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376585.6:c.878T>G	ENSP00000365770.1:p.Ile293Ser
ENST00000376590.9:c.755T>G MANE Select	ENSP00000365775.3:p.Ile252Ser
ENST00000376592.6:c.755T>G	ENSP00000365777.1:p.Ile252Ser
ENST00000423400.7:c.875T>G	ENSP00000398908.3:p.Ile292Ser
ENST00000641407.1:c.755T>G	ENSP00000493098.1:p.Ile252Ser
ENST00000641446.1:c.755T>G	ENSP00000493262.1:p.Ile252Ser
ENST00000641721.1:n.644-883T>G
ENST00000641747.1:c.*267T>G	ENSP00000493116.1:n.*267T>G
ENST00000641759.1:n.890T>G
ENST00000641805.1:n.1038T>G
ENST00000641820.1:c.20T>G	ENSP00000492937.1:p.Ile7Ser
ENST00000376583.7:c.878T>G	ENSP00000365767.3:p.Ile293Ser
ENST00000376585.5:c.878T>G	ENSP00000365770.1:p.Ile293Ser
ENST00000376590.7:c.755T>G	ENSP00000365775.3:p.Ile252Ser
ENST00000376592.5:c.755T>G	ENSP00000365777.1:p.Ile252Ser
NM_005957.4:c.755T>G , LRG_726t1:c.755T>G	NP_005948.3:p.Ile252Ser
XM_005263458.2:c.878T>G	XP_005263515.1:p.Ile293Ser
XM_005263460.3:c.755T>G	XP_005263517.1:p.Ile252Ser
XM_005263461.3:c.755T>G	XP_005263518.1:p.Ile252Ser
XM_005263462.3:c.755T>G	XP_005263519.1:p.Ile252Ser
XM_005263463.2:c.509T>G	XP_005263520.1:p.Ile170Ser
XM_011541495.1:c.875T>G	XP_011539797.1:p.Ile292Ser
XM_011541496.1:c.878T>G	XP_011539798.1:p.Ile293Ser
NM_001330358.1:c.878T>G	NP_001317287.1:p.Ile293Ser
XM_005263460.5:c.755T>G	XP_005263517.1:p.Ile252Ser
XM_005263462.4:c.755T>G	XP_005263519.1:p.Ile252Ser
XM_005263463.4:c.509T>G	XP_005263520.1:p.Ile170Ser
XM_011541495.3:c.875T>G	XP_011539797.1:p.Ile292Ser
XM_011541496.3:c.878T>G	XP_011539798.1:p.Ile293Ser
XM_017001328.2:c.878T>G	XP_016856817.1:p.Ile293Ser
XM_024447198.1:c.509T>G	XP_024302966.1:p.Ile170Ser
XR_002956640.1:n.1622T>G
NM_005957.5:c.755T>G MANE Select	NP_005948.3:p.Ile252Ser
NM_001330358.2:c.878T>G	NP_001317287.1:p.Ile293Ser