Canonical Allele Identifier: CA886038609

Gene: MTHFR C1orf167

Linked Data

• dbSNP Id: rs1292254673
• MyVariant Identifiers: chr1:g.11850279G>A (hg19) ; chr1:g.11790222G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11790222G>A , CM000663.2:g.11790222G>A	GRCh38
NC_000001.10:g.11850279G>A , CM000663.1:g.11850279G>A	GRCh37
NC_000001.9:g.11772866G>A	NCBI36
NG_013351.1:g.20882C>T , LRG_726:g.20882C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000376585.6:c.*458C>T (MTHFR)	ENSP00000365770.1:n.*458C>T
ENST00000376590.9:c.*458C>T (MTHFR) MANE Select	ENSP00000365775.3:n.*458C>T
ENST00000376592.6:c.*458C>T (MTHFR)	ENSP00000365777.1:n.*458C>T
ENST00000423400.7:c.*458C>T (MTHFR)	ENSP00000398908.3:n.*458C>T
ENST00000641446.1:c.*888C>T (MTHFR)	ENSP00000493262.1:n.*888C>T
ENST00000641747.1:c.*1941C>T (MTHFR)	ENSP00000493116.1:n.*1941C>T
ENST00000641805.1:n.2764C>T (MTHFR)
ENST00000376583.7:c.2552C>T (MTHFR)	ENSP00000365767.3:n.2552C>T
ENST00000376585.5:c.*458C>T (MTHFR)	ENSP00000365770.1:n.*458C>T
ENST00000376590.7:c.*458C>T (MTHFR)	ENSP00000365775.3:n.*458C>T
ENST00000376592.5:c.*458C>T (MTHFR)	ENSP00000365777.1:n.*458C>T
NM_005957.4:c.*458C>T , LRG_726t1:c.*458C>T (MTHFR)	NP_005948.3:n.*458C>T
XM_005263458.2:c.*458C>T (MTHFR)	XP_005263515.1:n.*458C>T
XM_005263460.3:c.*458C>T (MTHFR)	XP_005263517.1:n.*458C>T
XM_005263461.3:c.*458C>T (MTHFR)	XP_005263518.1:n.*458C>T
XM_005263462.3:c.*458C>T (MTHFR)	XP_005263519.1:n.*458C>T
XM_005263463.2:c.*458C>T (MTHFR)	XP_005263520.1:n.*458C>T
XM_011541495.1:c.*458C>T (MTHFR)	XP_011539797.1:n.*458C>T
XM_011541496.1:c.*318C>T (MTHFR)	XP_011539798.1:n.*318C>T
NM_001330358.1:c.*458C>T (MTHFR)	NP_001317287.1:n.*458C>T
XM_005263460.5:c.*458C>T (MTHFR)	XP_005263517.1:n.*458C>T
XM_005263462.4:c.*458C>T (MTHFR)	XP_005263519.1:n.*458C>T
XM_005263463.4:c.*458C>T (MTHFR)	XP_005263520.1:n.*458C>T
XM_011541272.3:c.*776G>A (C1orf167)	XP_011539574.1:n.*776G>A
XM_011541276.3:c.*763G>A (C1orf167)	XP_011539578.1:n.*763G>A
XM_011541277.3:c.*776G>A (C1orf167)	XP_011539579.1:n.*776G>A
XM_011541495.3:c.*458C>T (MTHFR)	XP_011539797.1:n.*458C>T
XM_011541496.3:c.*318C>T (MTHFR)	XP_011539798.1:n.*318C>T
XM_024446506.1:c.*1179G>A (C1orf167)	XP_024302274.1:n.*1179G>A
XM_024446507.1:c.*1179G>A (C1orf167)	XP_024302275.1:n.*1179G>A
XM_024446508.1:c.*1179G>A (C1orf167)	XP_024302276.1:n.*1179G>A
XM_024446509.1:c.*1179G>A (C1orf167)	XP_024302277.1:n.*1179G>A
XM_024446512.1:c.*1179G>A (C1orf167)	XP_024302280.1:n.*1179G>A
XM_024446514.1:c.*1179G>A (C1orf167)	XP_024302282.1:n.*1179G>A
XM_024446515.1:c.*1179G>A (C1orf167)	XP_024302283.1:n.*1179G>A
XM_024446517.1:c.*1179G>A (C1orf167)	XP_024302285.1:n.*1179G>A
XM_024446518.1:c.*1179G>A (C1orf167)	XP_024302286.1:n.*1179G>A
XM_024447198.1:c.*458C>T (MTHFR)	XP_024302966.1:n.*458C>T
NM_005957.5:c.*458C>T (MTHFR) MANE Select	NP_005948.3:n.*458C>T
NM_001330358.2:c.*458C>T (MTHFR)	NP_001317287.1:n.*458C>T