Canonical Allele Identifier: CA595283
Community Standard Title: NM_005957.5(MTHFR):c.1625A>C (p.Asn542Thr)
Gene: MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11792285T>G , CM000663.2:g.11792285T>G GRCh38
NC_000001.10:g.11852342T>G , CM000663.1:g.11852342T>G GRCh37
NC_000001.9:g.11774929T>G NCBI36
NG_013351.1:g.18819A>C , LRG_726:g.18819A>C

Transcript Alleles

HGVS Amino-acid Change
NM_005957.5:c.1625A>C MANE Select NP_005948.3:p.Asn542Thr
ENST00000376590.9:c.1625A>C MANE Select ENSP00000365775.3:p.Asn542Thr
NM_001330358.1:c.1748A>C NP_001317287.1:p.Asn583Thr
NM_001330358.2:c.1748A>C NP_001317287.1:p.Asn583Thr
NM_005957.4:c.1625A>C , LRG_726t1:c.1625A>C NP_005948.3:p.Asn542Thr
ENST00000376583.7:c.1748A>C ENSP00000365767.3:p.Asn583Thr
ENST00000376585.5:c.1748A>C ENSP00000365770.1:p.Asn583Thr
ENST00000376585.6:c.1748A>C ENSP00000365770.1:p.Asn583Thr
ENST00000376590.7:c.1625A>C ENSP00000365775.3:p.Asn542Thr
ENST00000376592.5:c.1625A>C ENSP00000365777.1:p.Asn542Thr
ENST00000376592.6:c.1625A>C ENSP00000365777.1:p.Asn542Thr
ENST00000423400.7:c.1745A>C ENSP00000398908.3:p.Asn582Thr
ENST00000641407.1:c.1625A>C ENSP00000493098.1:p.Asn542Thr
ENST00000641446.1:c.1625A>C ENSP00000493262.1:p.Asn542Thr
ENST00000641747.1:c.*1137A>C ENSP00000493116.1:n.*1137A>C
ENST00000641759.1:n.1994A>C
ENST00000641805.1:n.2142A>C
ENST00000641820.1:c.890A>C ENSP00000492937.1:p.Asn297Thr
XM_005263458.2:c.1748A>C XP_005263515.1:p.Asn583Thr
XM_005263460.3:c.1625A>C XP_005263517.1:p.Asn542Thr
XM_005263460.5:c.1625A>C XP_005263517.1:p.Asn542Thr
XM_005263461.3:c.1625A>C XP_005263518.1:p.Asn542Thr
XM_005263462.3:c.1625A>C XP_005263519.1:p.Asn542Thr
XM_005263462.4:c.1625A>C XP_005263519.1:p.Asn542Thr
XM_005263463.2:c.1379A>C XP_005263520.1:p.Asn460Thr
XM_005263463.4:c.1379A>C XP_005263520.1:p.Asn460Thr
XM_011541495.1:c.1745A>C XP_011539797.1:p.Asn582Thr
XM_011541495.3:c.1745A>C XP_011539797.1:p.Asn582Thr
XM_011541496.1:c.1748A>C XP_011539798.1:p.Asn583Thr
XM_011541496.3:c.1748A>C XP_011539798.1:p.Asn583Thr
XM_017001328.2:c.1748A>C XP_016856817.1:p.Asn583Thr
XM_024447198.1:c.1379A>C XP_024302966.1:p.Asn460Thr
XR_002956640.1:n.2726A>C