Canonical Allele Identifier: CA2742479631

Gene: MTHFR C1orf167

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11789872G>T , CM000663.2:g.11789872G>T	GRCh38
NC_000001.10:g.11849929G>T , CM000663.1:g.11849929G>T	GRCh37
NC_000001.9:g.11772516G>T	NCBI36
NG_013351.1:g.21232C>A , LRG_726:g.21232C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.*808C>A (MTHFR)	ENSP00000365770.1:n.*808C>A
ENST00000376590.9:c.*808C>A (MTHFR) MANE Select	ENSP00000365775.3:n.*808C>A
ENST00000376592.6:c.*808C>A (MTHFR)	ENSP00000365777.1:n.*808C>A
ENST00000641747.1:c.*2291C>A (MTHFR)	ENSP00000493116.1:n.*2291C>A
ENST00000376583.7:c.2902C>A (MTHFR)	ENSP00000365767.3:n.2902C>A
ENST00000376585.5:c.*808C>A (MTHFR)	ENSP00000365770.1:n.*808C>A
ENST00000376590.7:c.*808C>A (MTHFR)	ENSP00000365775.3:n.*808C>A
ENST00000376592.5:c.*808C>A (MTHFR)	ENSP00000365777.1:n.*808C>A
NM_005957.4:c.*808C>A , LRG_726t1:c.*808C>A (MTHFR)	NP_005948.3:n.*808C>A
NM_001330358.1:c.*808C>A (MTHFR)	NP_001317287.1:n.*808C>A
XM_011541272.3:c.*426G>T (C1orf167)	XP_011539574.1:n.*426G>T
XM_011541276.3:c.*413G>T (C1orf167)	XP_011539578.1:n.*413G>T
XM_011541277.3:c.*426G>T (C1orf167)	XP_011539579.1:n.*426G>T
XM_024446506.1:c.*829G>T (C1orf167)	XP_024302274.1:n.*829G>T
XM_024446507.1:c.*829G>T (C1orf167)	XP_024302275.1:n.*829G>T
XM_024446508.1:c.*829G>T (C1orf167)	XP_024302276.1:n.*829G>T
XM_024446509.1:c.*829G>T (C1orf167)	XP_024302277.1:n.*829G>T
XM_024446512.1:c.*829G>T (C1orf167)	XP_024302280.1:n.*829G>T
XM_024446514.1:c.*829G>T (C1orf167)	XP_024302282.1:n.*829G>T
XM_024446515.1:c.*829G>T (C1orf167)	XP_024302283.1:n.*829G>T
XM_024446517.1:c.*829G>T (C1orf167)	XP_024302285.1:n.*829G>T
XM_024446518.1:c.*829G>T (C1orf167)	XP_024302286.1:n.*829G>T
NM_005957.5:c.*808C>A (MTHFR) MANE Select	NP_005948.3:n.*808C>A
NM_001330358.2:c.*808C>A (MTHFR)	NP_001317287.1:n.*808C>A