Canonical Allele Identifier: CA595081

Gene: C1orf167 MTHFR

Linked Data

• dbSNP Id: rs555188130
• ExAC: 1:11848293 C / G
• gnomAD v2: 1-11848293-C-G
• gnomAD v3: 1-11788236-C-G
• gnomAD v4: 1-11788236-C-G
• MyVariant Identifiers: chr1:g.11848293C>G (hg19) ; chr1:g.11788236C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11788236C>G , CM000663.2:g.11788236C>G	GRCh38
NC_000001.10:g.11848293C>G , CM000663.1:g.11848293C>G	GRCh37
NC_000001.9:g.11770880C>G	NCBI36
NG_013351.1:g.22868G>C , LRG_726:g.22868G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433342.6:c.3435C>G (C1orf167)	ENSP00000414909.3:p.Gly1145=
ENST00000688073.1:c.3936C>G (C1orf167) MANE Select	ENSP00000510540.1:p.Gly1312=
ENST00000376585.6:c.*2444G>C (MTHFR)	ENSP00000365770.1:n.*2444G>C
ENST00000376590.9:c.*2444G>C (MTHFR) MANE Select	ENSP00000365775.3:n.*2444G>C
ENST00000376592.6:c.*2444G>C (MTHFR)	ENSP00000365777.1:n.*2444G>C
ENST00000312793.9:c.2071C>G (C1orf167)
ENST00000376583.7:c.4538G>C (MTHFR)	ENSP00000365767.3:n.4538G>C
ENST00000376590.7:c.*2444G>C (MTHFR)	ENSP00000365775.3:n.*2444G>C
ENST00000376592.5:c.*2444G>C (MTHFR)	ENSP00000365777.1:n.*2444G>C
ENST00000433342.5:c.3993C>G (C1orf167)	ENSP00000414909.2:p.Gly1331=
ENST00000444493.5:c.1435C>G (C1orf167)
ENST00000449278.1:c.1178-7C>G (C1orf167)
ENST00000482358.1:n.237-7C>G (C1orf167)
NM_001010881.1:c.3936C>G (C1orf167)	NP_001010881.1:p.Gly1312=
NM_005957.4:c.*2444G>C , LRG_726t1:c.*2444G>C (MTHFR)	NP_005948.3:n.*2444G>C
XM_006711078.2:c.3936C>G (C1orf167)	XP_006711141.1:p.Gly1312=
XM_011541267.1:c.4071C>G (C1orf167)	XP_011539569.1:p.Gly1357=
XM_011541268.1:c.4071C>G (C1orf167)	XP_011539570.1:p.Gly1357=
XM_011541269.1:c.4071C>G (C1orf167)	XP_011539571.1:p.Gly1357=
XM_011541270.1:c.4071C>G (C1orf167)	XP_011539572.1:p.Gly1357=
XM_011541271.1:c.4017C>G (C1orf167)	XP_011539573.1:p.Gly1339=
XM_011541272.1:c.4071C>G (C1orf167)	XP_011539574.1:p.Gly1357=
XM_011541273.1:c.3936C>G (C1orf167)	XP_011539575.1:p.Gly1312=
XM_011541274.1:c.3936C>G (C1orf167)	XP_011539576.1:p.Gly1312=
XM_011541275.1:c.3936C>G (C1orf167)	XP_011539577.1:p.Gly1312=
XM_011541276.1:c.3984-7C>G (C1orf167)	XP_011539578.1:n.3984-7C>G
XM_011541277.1:c.3984-7C>G (C1orf167)	XP_011539579.1:n.3984-7C>G
XM_011541278.1:c.4071C>G (C1orf167)	XP_011539580.1:p.Gly1357=
XM_011541279.1:c.3663C>G (C1orf167)	XP_011539581.1:p.Gly1221=
XM_011541280.1:c.2352C>G (C1orf167)	XP_011539582.1:p.Gly784=
XM_011541281.1:c.2352C>G (C1orf167)	XP_011539583.1:p.Gly784=
NM_001330358.1:c.*2444G>C (MTHFR)	NP_001317287.1:n.*2444G>C
XM_011541272.3:c.4071C>G (C1orf167)	XP_011539574.1:p.Gly1357=
XM_011541276.3:c.3984-7C>G (C1orf167)	XP_011539578.1:n.3984-7C>G
XM_011541277.3:c.3984-7C>G (C1orf167)	XP_011539579.1:n.3984-7C>G
XM_011541278.2:c.4071C>G (C1orf167)	XP_011539580.1:p.Gly1357=
XM_024446506.1:c.4071C>G (C1orf167)	XP_024302274.1:p.Gly1357=
XM_024446507.1:c.4071C>G (C1orf167)	XP_024302275.1:p.Gly1357=
XM_024446508.1:c.4071C>G (C1orf167)	XP_024302276.1:p.Gly1357=
XM_024446509.1:c.4071C>G (C1orf167)	XP_024302277.1:p.Gly1357=
XM_024446512.1:c.4017C>G (C1orf167)	XP_024302280.1:p.Gly1339=
XM_024446514.1:c.3936C>G (C1orf167)	XP_024302282.1:p.Gly1312=
XM_024446515.1:c.3936C>G (C1orf167)	XP_024302283.1:p.Gly1312=
XM_024446517.1:c.3936C>G (C1orf167)	XP_024302285.1:p.Gly1312=
XM_024446518.1:c.2352C>G (C1orf167)	XP_024302286.1:p.Gly784=
NM_001010881.2:c.3936C>G (C1orf167) MANE Select	NP_001010881.1:p.Gly1312=
NM_005957.5:c.*2444G>C (MTHFR) MANE Select	NP_005948.3:n.*2444G>C
NM_001330358.2:c.*2444G>C (MTHFR)	NP_001317287.1:n.*2444G>C