Canonical Allele Identifier: CA338470459

Gene: C1orf167 MTHFR

Linked Data

• dbSNP Id: rs1643961078
• gnomAD v4: 1-11788358-G-C
• MyVariant Identifiers: chr1:g.11848415G>C (hg19) ; chr1:g.11788358G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11788358G>C , CM000663.2:g.11788358G>C	GRCh38
NC_000001.10:g.11848415G>C , CM000663.1:g.11848415G>C	GRCh37
NC_000001.9:g.11771002G>C	NCBI36
NG_013351.1:g.22746C>G , LRG_726:g.22746C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433342.6:c.3557G>C (C1orf167)	ENSP00000414909.3:p.Arg1186Thr
ENST00000688073.1:c.4058G>C (C1orf167) MANE Select	ENSP00000510540.1:p.Arg1353Thr
ENST00000376585.6:c.*2322C>G (MTHFR)	ENSP00000365770.1:n.*2322C>G
ENST00000376590.9:c.*2322C>G (MTHFR) MANE Select	ENSP00000365775.3:n.*2322C>G
ENST00000376592.6:c.*2322C>G (MTHFR)	ENSP00000365777.1:n.*2322C>G
ENST00000312793.9:c.2193G>C (C1orf167)
ENST00000376583.7:c.4416C>G (MTHFR)	ENSP00000365767.3:n.4416C>G
ENST00000376585.5:c.*2322C>G (MTHFR)	ENSP00000365770.1:n.*2322C>G
ENST00000376590.7:c.*2322C>G (MTHFR)	ENSP00000365775.3:n.*2322C>G
ENST00000376592.5:c.*2322C>G (MTHFR)	ENSP00000365777.1:n.*2322C>G
ENST00000433342.5:c.4115G>C (C1orf167)	ENSP00000414909.2:p.Arg1372Thr
ENST00000444493.5:c.1557G>C (C1orf167)
ENST00000449278.1:c.1293G>C (C1orf167)
ENST00000482358.1:n.352G>C (C1orf167)
NM_001010881.1:c.4058G>C (C1orf167)	NP_001010881.1:p.Arg1353Thr
NM_005957.4:c.*2322C>G , LRG_726t1:c.*2322C>G (MTHFR)	NP_005948.3:n.*2322C>G
XM_006711078.2:c.4058G>C (C1orf167)	XP_006711141.1:p.Arg1353Thr
XM_011541267.1:c.4193G>C (C1orf167)	XP_011539569.1:p.Arg1398Thr
XM_011541268.1:c.4193G>C (C1orf167)	XP_011539570.1:p.Arg1398Thr
XM_011541269.1:c.4193G>C (C1orf167)	XP_011539571.1:p.Arg1398Thr
XM_011541270.1:c.4193G>C (C1orf167)	XP_011539572.1:p.Arg1398Thr
XM_011541271.1:c.4139G>C (C1orf167)	XP_011539573.1:p.Arg1380Thr
XM_011541272.1:c.4193G>C (C1orf167)	XP_011539574.1:p.Arg1398Thr
XM_011541273.1:c.4058G>C (C1orf167)	XP_011539575.1:p.Arg1353Thr
XM_011541274.1:c.4058G>C (C1orf167)	XP_011539576.1:p.Arg1353Thr
XM_011541275.1:c.4058G>C (C1orf167)	XP_011539577.1:p.Arg1353Thr
XM_011541276.1:c.4099G>C (C1orf167)	XP_011539578.1:p.Glu1367Gln
XM_011541277.1:c.4099G>C (C1orf167)	XP_011539579.1:p.Glu1367Gln
XM_011541278.1:c.4193G>C (C1orf167)	XP_011539580.1:p.Arg1398Thr
XM_011541279.1:c.3785G>C (C1orf167)	XP_011539581.1:p.Arg1262Thr
XM_011541280.1:c.2474G>C (C1orf167)	XP_011539582.1:p.Arg825Thr
XM_011541281.1:c.2474G>C (C1orf167)	XP_011539583.1:p.Arg825Thr
NM_001330358.1:c.*2322C>G (MTHFR)	NP_001317287.1:n.*2322C>G
XM_011541272.3:c.4193G>C (C1orf167)	XP_011539574.1:p.Arg1398Thr
XM_011541276.3:c.4099G>C (C1orf167)	XP_011539578.1:p.Glu1367Gln
XM_011541277.3:c.4099G>C (C1orf167)	XP_011539579.1:p.Glu1367Gln
XM_011541278.2:c.4193G>C (C1orf167)	XP_011539580.1:p.Arg1398Thr
XM_024446506.1:c.4193G>C (C1orf167)	XP_024302274.1:p.Arg1398Thr
XM_024446507.1:c.4193G>C (C1orf167)	XP_024302275.1:p.Arg1398Thr
XM_024446508.1:c.4193G>C (C1orf167)	XP_024302276.1:p.Arg1398Thr
XM_024446509.1:c.4193G>C (C1orf167)	XP_024302277.1:p.Arg1398Thr
XM_024446512.1:c.4139G>C (C1orf167)	XP_024302280.1:p.Arg1380Thr
XM_024446514.1:c.4058G>C (C1orf167)	XP_024302282.1:p.Arg1353Thr
XM_024446515.1:c.4058G>C (C1orf167)	XP_024302283.1:p.Arg1353Thr
XM_024446517.1:c.4058G>C (C1orf167)	XP_024302285.1:p.Arg1353Thr
XM_024446518.1:c.2474G>C (C1orf167)	XP_024302286.1:p.Arg825Thr
NM_001010881.2:c.4058G>C (C1orf167) MANE Select	NP_001010881.1:p.Arg1353Thr
NM_005957.5:c.*2322C>G (MTHFR) MANE Select	NP_005948.3:n.*2322C>G
NM_001330358.2:c.*2322C>G (MTHFR)	NP_001317287.1:n.*2322C>G