Canonical Allele Identifier: CA1140555801
Gene: C1orf167 HGNC NCBI
MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11787278_11787282delinsGAAGA , CM000663.2:g.11787278_11787282delinsGAAGA GRCh38
NC_000001.10:g.11847335_11847339delinsGAAGA , CM000663.1:g.11847335_11847339delinsGAAGA GRCh37
NC_000001.9:g.11769922_11769926delinsGAAGA NCBI36
NG_013351.1:g.23822_23826delinsTCTTC , LRG_726:g.23822_23826delinsTCTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000433342.6:c.3082-110_3082-106delinsGAAGA (C1orf167) ENSP00000414909.3:n.3082-110_3082-106delinsGAAGA
ENST00000688073.1:c.3568-110_3568-106delinsGAAGA (C1orf167) MANE Select ENSP00000510540.1:n.3568-110_3568-106delinsGAAGA
ENST00000376585.6:c.*3398_*3402delinsTCTTC (MTHFR) ENSP00000365770.1:n.*3398_*3402delinsTCTTC
ENST00000376590.9:c.*3398_*3402delinsTCTTC (MTHFR) MANE Select ENSP00000365775.3:n.*3398_*3402delinsTCTTC
ENST00000376592.6:c.*3398_*3402delinsTCTTC (MTHFR) ENSP00000365777.1:n.*3398_*3402delinsTCTTC
ENST00000312793.9:c.1718-110_1718-106delinsGAAGA (C1orf167)
ENST00000376583.7:c.5492_5496delinsTCTTC (MTHFR) ENSP00000365767.3:n.5492_5496delinsTCTTC
ENST00000376590.7:c.*3398_*3402delinsTCTTC (MTHFR) ENSP00000365775.3:n.*3398_*3402delinsTCTTC
ENST00000376592.5:c.*3398_*3402delinsTCTTC (MTHFR) ENSP00000365777.1:n.*3398_*3402delinsTCTTC
ENST00000433342.5:c.3640-110_3640-106delinsGAAGA (C1orf167) ENSP00000414909.2:n.3640-110_3640-106delinsGAAGA
ENST00000444493.5:c.1067-110_1067-106delinsGAAGA (C1orf167)
ENST00000449278.1:c.897-110_897-106delinsGAAGA (C1orf167)
ENST00000475041.1:n.120-110_120-106delinsGAAGA (C1orf167)
NM_001010881.1:c.3568-110_3568-106delinsGAAGA (C1orf167) NP_001010881.1:n.3568-110_3568-106delinsGAAGA
NM_005957.4:c.*3398_*3402delinsTCTTC , LRG_726t1:c.*3398_*3402delinsTCTTC (MTHFR) NP_005948.3:n.*3398_*3402delinsTCTTC
XM_006711078.2:c.3568-110_3568-106delinsGAAGA (C1orf167) XP_006711141.1:n.3568-110_3568-106delinsGAAGA
XM_011541267.1:c.3703-110_3703-106delinsGAAGA (C1orf167) XP_011539569.1:n.3703-110_3703-106delinsGAAGA
XM_011541268.1:c.3703-110_3703-106delinsGAAGA (C1orf167) XP_011539570.1:n.3703-110_3703-106delinsGAAGA
XM_011541269.1:c.3703-110_3703-106delinsGAAGA (C1orf167) XP_011539571.1:n.3703-110_3703-106delinsGAAGA
XM_011541270.1:c.3703-110_3703-106delinsGAAGA (C1orf167) XP_011539572.1:n.3703-110_3703-106delinsGAAGA
XM_011541271.1:c.3649-110_3649-106delinsGAAGA (C1orf167) XP_011539573.1:n.3649-110_3649-106delinsGAAGA
XM_011541272.1:c.3703-110_3703-106delinsGAAGA (C1orf167) XP_011539574.1:n.3703-110_3703-106delinsGAAGA
XM_011541273.1:c.3568-110_3568-106delinsGAAGA (C1orf167) XP_011539575.1:n.3568-110_3568-106delinsGAAGA
XM_011541274.1:c.3568-110_3568-106delinsGAAGA (C1orf167) XP_011539576.1:n.3568-110_3568-106delinsGAAGA
XM_011541275.1:c.3568-110_3568-106delinsGAAGA (C1orf167) XP_011539577.1:n.3568-110_3568-106delinsGAAGA
XM_011541276.1:c.3703-110_3703-106delinsGAAGA (C1orf167) XP_011539578.1:n.3703-110_3703-106delinsGAAGA
XM_011541277.1:c.3703-110_3703-106delinsGAAGA (C1orf167) XP_011539579.1:n.3703-110_3703-106delinsGAAGA
XM_011541278.1:c.3703-110_3703-106delinsGAAGA (C1orf167) XP_011539580.1:n.3703-110_3703-106delinsGAAGA
XM_011541279.1:c.3295-110_3295-106delinsGAAGA (C1orf167) XP_011539581.1:n.3295-110_3295-106delinsGAAGA
XM_011541280.1:c.1984-110_1984-106delinsGAAGA (C1orf167) XP_011539582.1:n.1984-110_1984-106delinsGAAGA
XM_011541281.1:c.1984-110_1984-106delinsGAAGA (C1orf167) XP_011539583.1:n.1984-110_1984-106delinsGAAGA
NM_001330358.1:c.*3398_*3402delinsTCTTC (MTHFR) NP_001317287.1:n.*3398_*3402delinsTCTTC
XM_011541272.3:c.3703-110_3703-106delinsGAAGA (C1orf167) XP_011539574.1:n.3703-110_3703-106delinsGAAGA
XM_011541276.3:c.3703-110_3703-106delinsGAAGA (C1orf167) XP_011539578.1:n.3703-110_3703-106delinsGAAGA
XM_011541277.3:c.3703-110_3703-106delinsGAAGA (C1orf167) XP_011539579.1:n.3703-110_3703-106delinsGAAGA
XM_011541278.2:c.3703-110_3703-106delinsGAAGA (C1orf167) XP_011539580.1:n.3703-110_3703-106delinsGAAGA
XM_024446506.1:c.3703-110_3703-106delinsGAAGA (C1orf167) XP_024302274.1:n.3703-110_3703-106delinsGAAGA
XM_024446507.1:c.3703-110_3703-106delinsGAAGA (C1orf167) XP_024302275.1:n.3703-110_3703-106delinsGAAGA
XM_024446508.1:c.3703-110_3703-106delinsGAAGA (C1orf167) XP_024302276.1:n.3703-110_3703-106delinsGAAGA
XM_024446509.1:c.3703-110_3703-106delinsGAAGA (C1orf167) XP_024302277.1:n.3703-110_3703-106delinsGAAGA
XM_024446512.1:c.3649-110_3649-106delinsGAAGA (C1orf167) XP_024302280.1:n.3649-110_3649-106delinsGAAGA
XM_024446514.1:c.3568-110_3568-106delinsGAAGA (C1orf167) XP_024302282.1:n.3568-110_3568-106delinsGAAGA
XM_024446515.1:c.3568-110_3568-106delinsGAAGA (C1orf167) XP_024302283.1:n.3568-110_3568-106delinsGAAGA
XM_024446517.1:c.3568-110_3568-106delinsGAAGA (C1orf167) XP_024302285.1:n.3568-110_3568-106delinsGAAGA
XM_024446518.1:c.1984-110_1984-106delinsGAAGA (C1orf167) XP_024302286.1:n.1984-110_1984-106delinsGAAGA
NM_001010881.2:c.3568-110_3568-106delinsGAAGA (C1orf167) MANE Select NP_001010881.1:n.3568-110_3568-106delinsGAAGA
NM_005957.5:c.*3398_*3402delinsTCTTC (MTHFR) MANE Select NP_005948.3:n.*3398_*3402delinsTCTTC
NM_001330358.2:c.*3398_*3402delinsTCTTC (MTHFR) NP_001317287.1:n.*3398_*3402delinsTCTTC