Canonical Allele Identifier: CA1147466073

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11790238A= , CM000663.2:g.11790238A=	GRCh38
NC_000001.10:g.11850295A= , CM000663.1:g.11850295A=	GRCh37
NC_000001.9:g.11772882A=	NCBI36
NG_013351.1:g.20866T= , LRG_726:g.20866T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376585.6:c.*442T=	ENSP00000365770.1:n.*442T=
ENST00000376590.9:c.*442T= MANE Select	ENSP00000365775.3:n.*442T=
ENST00000376592.6:c.*442T=	ENSP00000365777.1:n.*442T=
ENST00000423400.7:c.*442T=	ENSP00000398908.3:n.*442T=
ENST00000641446.1:c.*872T=	ENSP00000493262.1:n.*872T=
ENST00000641747.1:c.*1925T=	ENSP00000493116.1:n.*1925T=
ENST00000641805.1:n.2748T=
ENST00000376583.7:c.2536T=	ENSP00000365767.3:n.2536T=
ENST00000376585.5:c.*442T=	ENSP00000365770.1:n.*442T=
ENST00000376590.7:c.*442T=	ENSP00000365775.3:n.*442T=
ENST00000376592.5:c.*442T=	ENSP00000365777.1:n.*442T=
NM_005957.4:c.*442T= , LRG_726t1:c.*442T=	NP_005948.3:n.*442T=
XM_005263458.2:c.*442T=	XP_005263515.1:n.*442T=
XM_005263460.3:c.*442T=	XP_005263517.1:n.*442T=
XM_005263461.3:c.*442T=	XP_005263518.1:n.*442T=
XM_005263462.3:c.*442T=	XP_005263519.1:n.*442T=
XM_005263463.2:c.*442T=	XP_005263520.1:n.*442T=
XM_011541495.1:c.*442T=	XP_011539797.1:n.*442T=
XM_011541496.1:c.*302T=	XP_011539798.1:n.*302T=
NM_001330358.1:c.*442T=	NP_001317287.1:n.*442T=
XM_005263460.5:c.*442T=	XP_005263517.1:n.*442T=
XM_005263462.4:c.*442T=	XP_005263519.1:n.*442T=
XM_005263463.4:c.*442T=	XP_005263520.1:n.*442T=
XM_011541495.3:c.*442T=	XP_011539797.1:n.*442T=
XM_011541496.3:c.*302T=	XP_011539798.1:n.*302T=
XM_024447198.1:c.*442T=	XP_024302966.1:n.*442T=
NM_005957.5:c.*442T= MANE Select	NP_005948.3:n.*442T=
NM_001330358.2:c.*442T=	NP_001317287.1:n.*442T=