Canonical Allele Identifier: CA2643298659
Gene: MTHFR HGNC NCBI
C1orf167 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11790113del , CM000663.2:g.11790113del GRCh38
NC_000001.10:g.11850170del , CM000663.1:g.11850170del GRCh37
NC_000001.9:g.11772757del NCBI36
NG_013351.1:g.20993del , LRG_726:g.20993del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376585.6:c.*569del (MTHFR) ENSP00000365770.1:n.*569del
ENST00000376590.9:c.*569del (MTHFR) MANE Select ENSP00000365775.3:n.*569del
ENST00000376592.6:c.*569del (MTHFR) ENSP00000365777.1:n.*569del
ENST00000423400.7:c.*569del (MTHFR) ENSP00000398908.3:n.*569del
ENST00000641446.1:c.*999del (MTHFR) ENSP00000493262.1:n.*999del
ENST00000641747.1:c.*2052del (MTHFR) ENSP00000493116.1:n.*2052del
ENST00000641805.1:n.2875del (MTHFR)
ENST00000376583.7:c.2663del (MTHFR) ENSP00000365767.3:n.2663del
ENST00000376585.5:c.*569del (MTHFR) ENSP00000365770.1:n.*569del
ENST00000376590.7:c.*569del (MTHFR) ENSP00000365775.3:n.*569del
ENST00000376592.5:c.*569del (MTHFR) ENSP00000365777.1:n.*569del
NM_005957.4:c.*569del , LRG_726t1:c.*569del (MTHFR) NP_005948.3:n.*569del
XM_005263458.2:c.*569del (MTHFR) XP_005263515.1:n.*569del
XM_005263460.3:c.*569del (MTHFR) XP_005263517.1:n.*569del
XM_005263461.3:c.*569del (MTHFR) XP_005263518.1:n.*569del
XM_005263462.3:c.*569del (MTHFR) XP_005263519.1:n.*569del
XM_005263463.2:c.*569del (MTHFR) XP_005263520.1:n.*569del
XM_011541495.1:c.*569del (MTHFR) XP_011539797.1:n.*569del
XM_011541496.1:c.*429del (MTHFR) XP_011539798.1:n.*429del
NM_001330358.1:c.*569del (MTHFR) NP_001317287.1:n.*569del
XM_005263460.5:c.*569del (MTHFR) XP_005263517.1:n.*569del
XM_005263462.4:c.*569del (MTHFR) XP_005263519.1:n.*569del
XM_005263463.4:c.*569del (MTHFR) XP_005263520.1:n.*569del
XM_011541272.3:c.*667del (C1orf167) XP_011539574.1:n.*667del
XM_011541276.3:c.*654del (C1orf167) XP_011539578.1:n.*654del
XM_011541277.3:c.*667del (C1orf167) XP_011539579.1:n.*667del
XM_011541495.3:c.*569del (MTHFR) XP_011539797.1:n.*569del
XM_011541496.3:c.*429del (MTHFR) XP_011539798.1:n.*429del
XM_024446506.1:c.*1070del (C1orf167) XP_024302274.1:n.*1070del
XM_024446507.1:c.*1070del (C1orf167) XP_024302275.1:n.*1070del
XM_024446508.1:c.*1070del (C1orf167) XP_024302276.1:n.*1070del
XM_024446509.1:c.*1070del (C1orf167) XP_024302277.1:n.*1070del
XM_024446512.1:c.*1070del (C1orf167) XP_024302280.1:n.*1070del
XM_024446514.1:c.*1070del (C1orf167) XP_024302282.1:n.*1070del
XM_024446515.1:c.*1070del (C1orf167) XP_024302283.1:n.*1070del
XM_024446517.1:c.*1070del (C1orf167) XP_024302285.1:n.*1070del
XM_024446518.1:c.*1070del (C1orf167) XP_024302286.1:n.*1070del
XM_024447198.1:c.*569del (MTHFR) XP_024302966.1:n.*569del
NM_005957.5:c.*569del (MTHFR) MANE Select NP_005948.3:n.*569del
NM_001330358.2:c.*569del (MTHFR) NP_001317287.1:n.*569del