Canonical Allele Identifier: CA1153789306

Gene: MTHFR C1orf167

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11789845G= , CM000663.2:g.11789845G=	GRCh38
NC_000001.10:g.11849902G= , CM000663.1:g.11849902G=	GRCh37
NC_000001.9:g.11772489G=	NCBI36
NG_013351.1:g.21259C= , LRG_726:g.21259C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.*835C= (MTHFR)	ENSP00000365770.1:n.*835C=
ENST00000376590.9:c.*835C= (MTHFR) MANE Select	ENSP00000365775.3:n.*835C=
ENST00000376592.6:c.*835C= (MTHFR)	ENSP00000365777.1:n.*835C=
ENST00000641747.1:c.*2318C= (MTHFR)	ENSP00000493116.1:n.*2318C=
ENST00000376583.7:c.2929C= (MTHFR)	ENSP00000365767.3:n.2929C=
ENST00000376585.5:c.*835C= (MTHFR)	ENSP00000365770.1:n.*835C=
ENST00000376590.7:c.*835C= (MTHFR)	ENSP00000365775.3:n.*835C=
ENST00000376592.5:c.*835C= (MTHFR)	ENSP00000365777.1:n.*835C=
NM_005957.4:c.*835C= , LRG_726t1:c.*835C= (MTHFR)	NP_005948.3:n.*835C=
NM_001330358.1:c.*835C= (MTHFR)	NP_001317287.1:n.*835C=
XM_011541272.3:c.*399G= (C1orf167)	XP_011539574.1:n.*399G=
XM_011541276.3:c.*386G= (C1orf167)	XP_011539578.1:n.*386G=
XM_011541277.3:c.*399G= (C1orf167)	XP_011539579.1:n.*399G=
XM_024446506.1:c.*802G= (C1orf167)	XP_024302274.1:n.*802G=
XM_024446507.1:c.*802G= (C1orf167)	XP_024302275.1:n.*802G=
XM_024446508.1:c.*802G= (C1orf167)	XP_024302276.1:n.*802G=
XM_024446509.1:c.*802G= (C1orf167)	XP_024302277.1:n.*802G=
XM_024446512.1:c.*802G= (C1orf167)	XP_024302280.1:n.*802G=
XM_024446514.1:c.*802G= (C1orf167)	XP_024302282.1:n.*802G=
XM_024446515.1:c.*802G= (C1orf167)	XP_024302283.1:n.*802G=
XM_024446517.1:c.*802G= (C1orf167)	XP_024302285.1:n.*802G=
XM_024446518.1:c.*802G= (C1orf167)	XP_024302286.1:n.*802G=
NM_005957.5:c.*835C= (MTHFR) MANE Select	NP_005948.3:n.*835C=
NM_001330358.2:c.*835C= (MTHFR)	NP_001317287.1:n.*835C=