Canonical Allele Identifier: CA338473344

Gene: MTHFR

Linked Data

• MyVariant Identifiers: chr1:g.11850806C>G (hg19) ; chr1:g.11790749C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11790749C>G , CM000663.2:g.11790749C>G	GRCh38
NC_000001.10:g.11850806C>G , CM000663.1:g.11850806C>G	GRCh37
NC_000001.9:g.11773393C>G	NCBI36
NG_013351.1:g.20355G>C , LRG_726:g.20355G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376585.6:c.2025G>C	ENSP00000365770.1:p.Gln675His
ENST00000376590.9:c.1902G>C MANE Select	ENSP00000365775.3:p.Gln634His
ENST00000376592.6:c.1902G>C	ENSP00000365777.1:p.Gln634His
ENST00000423400.7:c.2022G>C	ENSP00000398908.3:p.Gln674His
ENST00000641407.1:c.1753-33G>C	ENSP00000493098.1:n.1753-33G>C
ENST00000641446.1:c.*361G>C	ENSP00000493262.1:n.*361G>C
ENST00000641747.1:c.*1414G>C	ENSP00000493116.1:n.*1414G>C
ENST00000641759.1:n.2271G>C
ENST00000641805.1:n.2270-33G>C
ENST00000641820.1:c.1167G>C	ENSP00000492937.1:p.Gln389His
ENST00000376583.7:c.2025G>C	ENSP00000365767.3:p.Gln675His
ENST00000376585.5:c.2025G>C	ENSP00000365770.1:p.Gln675His
ENST00000376590.7:c.1902G>C	ENSP00000365775.3:p.Gln634His
ENST00000376592.5:c.1902G>C	ENSP00000365777.1:p.Gln634His
NM_005957.4:c.1902G>C , LRG_726t1:c.1902G>C	NP_005948.3:p.Gln634His
XM_005263458.2:c.2025G>C	XP_005263515.1:p.Gln675His
XM_005263460.3:c.1902G>C	XP_005263517.1:p.Gln634His
XM_005263461.3:c.1902G>C	XP_005263518.1:p.Gln634His
XM_005263462.3:c.1902G>C	XP_005263519.1:p.Gln634His
XM_005263463.2:c.1656G>C	XP_005263520.1:p.Gln552His
XM_011541495.1:c.2022G>C	XP_011539797.1:p.Gln674His
XM_011541496.1:c.1876-33G>C	XP_011539798.1:n.1876-33G>C
NM_001330358.1:c.2025G>C	NP_001317287.1:p.Gln675His
XM_005263460.5:c.1902G>C	XP_005263517.1:p.Gln634His
XM_005263462.4:c.1902G>C	XP_005263519.1:p.Gln634His
XM_005263463.4:c.1656G>C	XP_005263520.1:p.Gln552His
XM_011541495.3:c.2022G>C	XP_011539797.1:p.Gln674His
XM_011541496.3:c.1876-33G>C	XP_011539798.1:n.1876-33G>C
XM_017001328.2:c.1876-1G>C	XP_016856817.1:n.1876-1G>C
XM_024447198.1:c.1656G>C	XP_024302966.1:p.Gln552His
XR_002956640.1:n.2854-33G>C
NM_005957.5:c.1902G>C MANE Select	NP_005948.3:p.Gln634His
NM_001330358.2:c.2025G>C	NP_001317287.1:p.Gln675His